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p-content-read table-responsive">content-read table-responsive">ntent-read table-responsive">t-read table-responsive">read table-responsive">ad table-responsive">stickerickerker id classasss="txtnds whose molecules contain more than one multiple (double or triple) bonds. According to mutual arrangement, the multiple bonds of polyunsaturated compounds are classified as being cumulated, isolated, and conjugated. These will be considered by the simplest examples, namely, alkadienes that are usually referred to simply as dienes.s whose molecules contain more than one multiple (double or triple) bonds. According to mutual arrangement, the multiple bonds of polyunsaturated compounds are classified as being cumulated, isolated, and conjugated. These will be considered by the simplest examples, namely, alkadienes that are usually referred to simply as dienes.whose molecules contain more than one multiple (double or triple) bonds. According to mutual arrangement, the multiple bonds of polyunsaturated compounds are classified as being cumulated, isolated, and conjugated. These will be considered by the simplest examples, namely, alkadienes that are usually referred to simply as dienes.ose molecules contain more than one multiple (double or triple) bonds. According to mutual arrangement, the multiple bonds of polyunsaturated compounds are classified as being cumulated, isolated, and conjugated. These will be considered by the simplest examples, namely, alkadienes that are usually referred to simply as dienes.olecules contain more than one multiple (double or triple) bonds. According to mutual arrangement, the multiple bonds of polyunsaturated compounds are classified as being cumulated, isolated, and conjugated. These will be considered by the simplest examples, namely, alkadienes that are usually referred to simply as dienes.ecules contain more than one multiple (double or triple) bonds. According to mutual arrangement, the multiple bonds of polyunsaturated compounds are classified as being cumulated, isolated, and conjugated. These will be considered by the simplest examples, namely, alkadienes that are usually referred to simply as dienes.ules contain more than one multiple (double or triple) bonds. According to mutual arrangement, the multiple bonds of polyunsaturated compounds are classified as being cumulated, isolated, and conjugated. These will be considered by the simplest examples, namely, alkadienes that are usually referred to simply as dienes. to mutual arrangement, the multiple bonds of polyunsaturated compounds are classified as being cumulated, isolated, and conjugated. These will be considered by the simplest examples, namely, alkadienes that are usually referred to simply as dienes.o mutual arrangement, the multiple bonds of polyunsaturated compounds are classified as being cumulated, isolated, and conjugated. These will be considered by the simplest examples, namely, alkadienes that are usually referred to simply as dienes.mutual arrangement, the multiple bonds of polyunsaturated compounds are classified as being cumulated, isolated, and conjugated. These will be considered by the simplest examples, namely, alkadienes that are usually referred to simply as dienes.tual arrangement, the multiple bonds of polyunsaturated compounds are classified as being cumulated, isolated, and conjugated. These will be considered by the simplest examples, namely, alkadienes that are usually referred to simply as dienes. arrangement, the multiple bonds of polyunsaturated compounds are classified as being cumulated, isolated, and conjugated. These will be considered by the simplest examples, namely, alkadienes that are usually referred to simply as dienes.rrangement, the multiple bonds of polyunsaturated compounds are classified as being cumulated, isolated, and conjugated. These will be considered by the simplest examples, namely, alkadienes that are usually referred to simply as dienes.gement, the multiple bonds of polyunsaturated compounds are classified as being cumulated, isolated, and conjugated. These will be considered by the simplest examples, namely, alkadienes that are usually referred to simply as dienes.ment, the multiple bonds of polyunsaturated compounds are classified as being cumulated, isolated, and conjugated. These will be considered by the simplest examples, namely, alkadienes that are usually referred to simply as dienes.nt, the multiple bonds of polyunsaturated compounds are classified as being cumulated, isolated, and conjugated. These will be considered by the simplest examples, namely, alkadienes that are usually referred to simply as dienes. as being cumulated, isolated, and conjugated. These will be considered by the simplest examples, namely, alkadienes that are usually referred to simply as dienes.s being cumulated, isolated, and conjugated. These will be considered by the simplest examples, namely, alkadienes that are usually referred to simply as dienes.being cumulated, isolated, and conjugated. These will be considered by the simplest examples, namely, alkadienes that are usually referred to simply as dienes.g cumulated, isolated, and conjugated. These will be considered by the simplest examples, namely, alkadienes that are usually referred to simply as dienes.cumulated, isolated, and conjugated. These will be considered by the simplest examples, namely, alkadienes that are usually referred to simply as dienes.>cumulated, isolated, and conjugated. These will be considered by the simplest examples, namely, alkadienes that are usually referred to simply as dienes.ed. These will be considered by the simplest examples, namely, alkadienes that are usually referred to simply as dienes.. These will be considered by the simplest examples, namely, alkadienes that are usually referred to simply as dienes.These will be considered by the simplest examples, namely, alkadienes that are usually referred to simply as dienes.ese will be considered by the simplest examples, namely, alkadienes that are usually referred to simply as dienes.e will be considered by the simplest examples, namely, alkadienes that are usually referred to simply as dienes.will be considered by the simplest examples, namely, alkadienes that are usually referred to simply as dienes.es, namely, alkadienes that are usually referred to simply as dienes., namely, alkadienes that are usually referred to simply as dienes.namely, alkadienes that are usually referred to simply as dienes.mely, alkadienes that are usually referred to simply as dienes.ly, alkadienes that are usually referred to simply as dienes., alkadienes that are usually referred to simply as dienes.alkadienes that are usually referred to simply as dienes.ienes.nes.s./span>pan>n>/prior.studentlibrary.ru/cgi-bin/mb4x?usr_data=gd-image(doc,ISBN9785970434437-0003,pic_0065.jpg,-1,,00000000,)&hide_Cookie=yes" asis-dx="531" asis-dy="77">rior.studentlibrary.ru/cgi-bin/mb4x?usr_data=gd-image(doc,ISBN9785970434437-0003,pic_0065.jpg,-1,,00000000,)&hide_Cookie=yes" asis-dx="531" asis-dy="77">or.studentlibrary.ru/cgi-bin/mb4x?usr_data=gd-image(doc,ISBN9785970434437-0003,pic_0065.jpg,-1,,00000000,)&hide_Cookie=yes" asis-dx="531" asis-dy="77">.studentlibrary.ru/cgi-bin/mb4x?usr_data=gd-image(doc,ISBN9785970434437-0003,pic_0065.jpg,-1,,00000000,)&hide_Cookie=yes" asis-dx="531" asis-dy="77">dentlibrary.ru/cgi-bin/mb4x?usr_data=gd-image(doc,ISBN9785970434437-0003,pic_0065.jpg,-1,,00000000,)&hide_Cookie=yes" asis-dx="531" asis-dy="77">ntlibrary.ru/cgi-bin/mb4x?usr_data=gd-image(doc,ISBN9785970434437-0003,pic_0065.jpg,-1,,00000000,)&hide_Cookie=yes" asis-dx="531" asis-dy="77">brary.ru/cgi-bin/mb4x?usr_data=gd-image(doc,ISBN9785970434437-0003,pic_0065.jpg,-1,,00000000,)&hide_Cookie=yes" asis-dx="531" asis-dy="77">ary.ru/cgi-bin/mb4x?usr_data=gd-image(doc,ISBN9785970434437-0003,pic_0065.jpg,-1,,00000000,)&hide_Cookie=yes" asis-dx="531" asis-dy="77">y.ru/cgi-bin/mb4x?usr_data=gd-image(doc,ISBN9785970434437-0003,pic_0065.jpg,-1,,00000000,)&hide_Cookie=yes" asis-dx="531" asis-dy="77">65.jpg,-1,,00000000,)&hide_Cookie=yes" asis-dx="531" asis-dy="77">.jpg,-1,,00000000,)&hide_Cookie=yes" asis-dx="531" asis-dy="77">pg,-1,,00000000,)&hide_Cookie=yes" asis-dx="531" asis-dy="77">1,,00000000,)&hide_Cookie=yes" asis-dx="531" asis-dy="77">,00000000,)&hide_Cookie=yes" asis-dx="531" asis-dy="77">0000000,)&hide_Cookie=yes" asis-dx="531" asis-dy="77">"531" asis-dy="77">31" asis-dy="77">" asis-dy="77">-dy="77">y="77">"77">"txtt">The term cumulated means that one carbon participates in two double bonds; in other words, these bonds follow one after another. This type of bonding occurs very rarely among the natural products. If at least one saturated carbon atom intervenes between the double bonds of a diene, these bonds are regarded as isolated. Thus, 1,2-butadiene is an example of cumulated dienes, and 1,4-pentadiene represents isolated dienes.pan class="">The term cumulated means that one carbon participates in two double bonds; in other words, these bonds follow one after another. This type of bonding occurs very rarely among the natural products. If at least one saturated carbon atom intervenes between the double bonds of a diene, these bonds are regarded as isolated. Thus, 1,2-butadiene is an example of cumulated dienes, and 1,4-pentadiene represents isolated dienes.e carbon participates in two double bonds; in other words, these bonds follow one after another. This type of bonding occurs very rarely among the natural products. If at least one saturated carbon atom intervenes between the double bonds of a diene, these bonds are regarded as isolated. Thus, 1,2-butadiene is an example of cumulated dienes, and 1,4-pentadiene represents isolated dienes.carbon participates in two double bonds; in other words, these bonds follow one after another. This type of bonding occurs very rarely among the natural products. If at least one saturated carbon atom intervenes between the double bonds of a diene, these bonds are regarded as isolated. Thus, 1,2-butadiene is an example of cumulated dienes, and 1,4-pentadiene represents isolated dienes.rbon participates in two double bonds; in other words, these bonds follow one after another. This type of bonding occurs very rarely among the natural products. If at least one saturated carbon atom intervenes between the double bonds of a diene, these bonds are regarded as isolated. Thus, 1,2-butadiene is an example of cumulated dienes, and 1,4-pentadiene represents isolated dienes.on participates in two double bonds; in other words, these bonds follow one after another. This type of bonding occurs very rarely among the natural products. If at least one saturated carbon atom intervenes between the double bonds of a diene, these bonds are regarded as isolated. Thus, 1,2-butadiene is an example of cumulated dienes, and 1,4-pentadiene represents isolated dienes.rticipates in two double bonds; in other words, these bonds follow one after another. This type of bonding occurs very rarely among the natural products. If at least one saturated carbon atom intervenes between the double bonds of a diene, these bonds are regarded as isolated. Thus, 1,2-butadiene is an example of cumulated dienes, and 1,4-pentadiene represents isolated dienes.icipates in two double bonds; in other words, these bonds follow one after another. This type of bonding occurs very rarely among the natural products. If at least one saturated carbon atom intervenes between the double bonds of a diene, these bonds are regarded as isolated. Thus, 1,2-butadiene is an example of cumulated dienes, and 1,4-pentadiene represents isolated dienes.ipates in two double bonds; in other words, these bonds follow one after another. This type of bonding occurs very rarely among the natural products. If at least one saturated carbon atom intervenes between the double bonds of a diene, these bonds are regarded as isolated. Thus, 1,2-butadiene is an example of cumulated dienes, and 1,4-pentadiene represents isolated dienes.r another. This type of bonding occurs very rarely among the natural products. If at least one saturated carbon atom intervenes between the double bonds of a diene, these bonds are regarded as isolated. Thus, 1,2-butadiene is an example of cumulated dienes, and 1,4-pentadiene represents isolated dienes.another. This type of bonding occurs very rarely among the natural products. If at least one saturated carbon atom intervenes between the double bonds of a diene, these bonds are regarded as isolated. Thus, 1,2-butadiene is an example of cumulated dienes, and 1,4-pentadiene represents isolated dienes.other. This type of bonding occurs very rarely among the natural products. If at least one saturated carbon atom intervenes between the double bonds of a diene, these bonds are regarded as isolated. Thus, 1,2-butadiene is an example of cumulated dienes, and 1,4-pentadiene represents isolated dienes.her. This type of bonding occurs very rarely among the natural products. If at least one saturated carbon atom intervenes between the double bonds of a diene, these bonds are regarded as isolated. Thus, 1,2-butadiene is an example of cumulated dienes, and 1,4-pentadiene represents isolated dienes. This type of bonding occurs very rarely among the natural products. If at least one saturated carbon atom intervenes between the double bonds of a diene, these bonds are regarded as isolated. Thus, 1,2-butadiene is an example of cumulated dienes, and 1,4-pentadiene represents isolated dienes.his type of bonding occurs very rarely among the natural products. If at least one saturated carbon atom intervenes between the double bonds of a diene, these bonds are regarded as isolated. Thus, 1,2-butadiene is an example of cumulated dienes, and 1,4-pentadiene represents isolated dienes.type of bonding occurs very rarely among the natural products. If at least one saturated carbon atom intervenes between the double bonds of a diene, these bonds are regarded as isolated. Thus, 1,2-butadiene is an example of cumulated dienes, and 1,4-pentadiene represents isolated dienes.pe of bonding occurs very rarely among the natural products. If at least one saturated carbon atom intervenes between the double bonds of a diene, these bonds are regarded as isolated. Thus, 1,2-butadiene is an example of cumulated dienes, and 1,4-pentadiene represents isolated dienes. of bonding occurs very rarely among the natural products. If at least one saturated carbon atom intervenes between the double bonds of a diene, these bonds are regarded as isolated. Thus, 1,2-butadiene is an example of cumulated dienes, and 1,4-pentadiene represents isolated dienes.st one saturated carbon atom intervenes between the double bonds of a diene, these bonds are regarded as isolated. Thus, 1,2-butadiene is an example of cumulated dienes, and 1,4-pentadiene represents isolated dienes. one saturated carbon atom intervenes between the double bonds of a diene, these bonds are regarded as isolated. Thus, 1,2-butadiene is an example of cumulated dienes, and 1,4-pentadiene represents isolated dienes.ne saturated carbon atom intervenes between the double bonds of a diene, these bonds are regarded as isolated. Thus, 1,2-butadiene is an example of cumulated dienes, and 1,4-pentadiene represents isolated dienes.aturated carbon atom intervenes between the double bonds of a diene, these bonds are regarded as isolated. Thus, 1,2-butadiene is an example of cumulated dienes, and 1,4-pentadiene represents isolated dienes.urated carbon atom intervenes between the double bonds of a diene, these bonds are regarded as isolated. Thus, 1,2-butadiene is an example of cumulated dienes, and 1,4-pentadiene represents isolated dienes.ated carbon atom intervenes between the double bonds of a diene, these bonds are regarded as isolated. Thus, 1,2-butadiene is an example of cumulated dienes, and 1,4-pentadiene represents isolated dienes.ouble bonds of a diene, these bonds are regarded as isolated. Thus, 1,2-butadiene is an example of cumulated dienes, and 1,4-pentadiene represents isolated dienes.ble bonds of a diene, these bonds are regarded as isolated. Thus, 1,2-butadiene is an example of cumulated dienes, and 1,4-pentadiene represents isolated dienes.e bonds of a diene, these bonds are regarded as isolated. Thus, 1,2-butadiene is an example of cumulated dienes, and 1,4-pentadiene represents isolated dienes.s of a diene, these bonds are regarded as isolated. Thus, 1,2-butadiene is an example of cumulated dienes, and 1,4-pentadiene represents isolated dienes.of a diene, these bonds are regarded as isolated. Thus, 1,2-butadiene is an example of cumulated dienes, and 1,4-pentadiene represents isolated dienes. a diene, these bonds are regarded as isolated. Thus, 1,2-butadiene is an example of cumulated dienes, and 1,4-pentadiene represents isolated dienes.lated. Thus, 1,2-butadiene is an example of cumulated dienes, and 1,4-pentadiene represents isolated dienes.ted. Thus, 1,2-butadiene is an example of cumulated dienes, and 1,4-pentadiene represents isolated dienes.d. Thus, 1,2-butadiene is an example of cumulated dienes, and 1,4-pentadiene represents isolated dienes. Thus, 1,2-butadiene is an example of cumulated dienes, and 1,4-pentadiene represents isolated dienes.hus, 1,2-butadiene is an example of cumulated dienes, and 1,4-pentadiene represents isolated dienes.s, 1,2-butadiene is an example of cumulated dienes, and 1,4-pentadiene represents isolated dienes. 1,2-butadiene is an example of cumulated dienes, and 1,4-pentadiene represents isolated dienes./span>pan>n>p>-carotene is a yellow-orange pigment in carrots that involves eleven conjugated double bonds:urated compounds with conjugated double bonds, which play an important role in nature and biology. For example, β-carotene is a yellow-orange pigment in carrots that involves eleven conjugated double bonds:ated compounds with conjugated double bonds, which play an important role in nature and biology. For example, β-carotene is a yellow-orange pigment in carrots that involves eleven conjugated double bonds:ed compounds with conjugated double bonds, which play an important role in nature and biology. For example, β-carotene is a yellow-orange pigment in carrots that involves eleven conjugated double bonds:ompounds with conjugated double bonds, which play an important role in nature and biology. For example, β-carotene is a yellow-orange pigment in carrots that involves eleven conjugated double bonds:pounds with conjugated double bonds, which play an important role in nature and biology. For example, β-carotene is a yellow-orange pigment in carrots that involves eleven conjugated double bonds:ds with conjugated double bonds, which play an important role in nature and biology. For example, β-carotene is a yellow-orange pigment in carrots that involves eleven conjugated double bonds: with conjugated double bonds, which play an important role in nature and biology. For example, β-carotene is a yellow-orange pigment in carrots that involves eleven conjugated double bonds:ith conjugated double bonds, which play an important role in nature and biology. For example, β-carotene is a yellow-orange pigment in carrots that involves eleven conjugated double bonds:t role in nature and biology. For example, β-carotene is a yellow-orange pigment in carrots that involves eleven conjugated double bonds:role in nature and biology. For example, β-carotene is a yellow-orange pigment in carrots that involves eleven conjugated double bonds:le in nature and biology. For example, β-carotene is a yellow-orange pigment in carrots that involves eleven conjugated double bonds:n nature and biology. For example, β-carotene is a yellow-orange pigment in carrots that involves eleven conjugated double bonds:nature and biology. For example, β-carotene is a yellow-orange pigment in carrots that involves eleven conjugated double bonds:ture and biology. For example, β-carotene is a yellow-orange pigment in carrots that involves eleven conjugated double bonds:e, β-carotene is a yellow-orange pigment in carrots that involves eleven conjugated double bonds: β-carotene is a yellow-orange pigment in carrots that involves eleven conjugated double bonds:�-carotene is a yellow-orange pigment in carrots that involves eleven conjugated double bonds:arotene is a yellow-orange pigment in carrots that involves eleven conjugated double bonds:otene is a yellow-orange pigment in carrots that involves eleven conjugated double bonds:ene is a yellow-orange pigment in carrots that involves eleven conjugated double bonds:igment in carrots that involves eleven conjugated double bonds:ment in carrots that involves eleven conjugated double bonds:nt in carrots that involves eleven conjugated double bonds: in carrots that involves eleven conjugated double bonds:n carrots that involves eleven conjugated double bonds:carrots that involves eleven conjugated double bonds:rrots that involves eleven conjugated double bonds:s:an>>/p>entlibrary.ru/cgi-bin/mb4x?usr_data=gd-image(doc,ISBN9785970434437-0003,pic_0066.jpg,-1,,00000000,)&hide_Cookie=yes" asis-dx="531" asis-dy="159">tlibrary.ru/cgi-bin/mb4x?usr_data=gd-image(doc,ISBN9785970434437-0003,pic_0066.jpg,-1,,00000000,)&hide_Cookie=yes" asis-dx="531" asis-dy="159">ibrary.ru/cgi-bin/mb4x?usr_data=gd-image(doc,ISBN9785970434437-0003,pic_0066.jpg,-1,,00000000,)&hide_Cookie=yes" asis-dx="531" asis-dy="159">ry.ru/cgi-bin/mb4x?usr_data=gd-image(doc,ISBN9785970434437-0003,pic_0066.jpg,-1,,00000000,)&hide_Cookie=yes" asis-dx="531" asis-dy="159">.ru/cgi-bin/mb4x?usr_data=gd-image(doc,ISBN9785970434437-0003,pic_0066.jpg,-1,,00000000,)&hide_Cookie=yes" asis-dx="531" asis-dy="159">u/cgi-bin/mb4x?usr_data=gd-image(doc,ISBN9785970434437-0003,pic_0066.jpg,-1,,00000000,)&hide_Cookie=yes" asis-dx="531" asis-dy="159">/cgi-bin/mb4x?usr_data=gd-image(doc,ISBN9785970434437-0003,pic_0066.jpg,-1,,00000000,)&hide_Cookie=yes" asis-dx="531" asis-dy="159">gi-bin/mb4x?usr_data=gd-image(doc,ISBN9785970434437-0003,pic_0066.jpg,-1,,00000000,)&hide_Cookie=yes" asis-dx="531" asis-dy="159">-bin/mb4x?usr_data=gd-image(doc,ISBN9785970434437-0003,pic_0066.jpg,-1,,00000000,)&hide_Cookie=yes" asis-dx="531" asis-dy="159">b4x?usr_data=gd-image(doc,ISBN9785970434437-0003,pic_0066.jpg,-1,,00000000,)&hide_Cookie=yes" asis-dx="531" asis-dy="159">x?usr_data=gd-image(doc,ISBN9785970434437-0003,pic_0066.jpg,-1,,00000000,)&hide_Cookie=yes" asis-dx="531" asis-dy="159">usr_data=gd-image(doc,ISBN9785970434437-0003,pic_0066.jpg,-1,,00000000,)&hide_Cookie=yes" asis-dx="531" asis-dy="159">sr_data=gd-image(doc,ISBN9785970434437-0003,pic_0066.jpg,-1,,00000000,)&hide_Cookie=yes" asis-dx="531" asis-dy="159">_data=gd-image(doc,ISBN9785970434437-0003,pic_0066.jpg,-1,,00000000,)&hide_Cookie=yes" asis-dx="531" asis-dy="159">ata=gd-image(doc,ISBN9785970434437-0003,pic_0066.jpg,-1,,00000000,)&hide_Cookie=yes" asis-dx="531" asis-dy="159">34437-0003,pic_0066.jpg,-1,,00000000,)&hide_Cookie=yes" asis-dx="531" asis-dy="159">t"Other examples of highly conjugated systems among biologically active compounds are retinol (vitamin A) and retinal, the latter being a substance responsible for vision.pan class="">Other examples of highly conjugated systems among biologically active compounds are retinol (vitamin A) and retinal, the latter being a substance responsible for vision.ass="">Other examples of highly conjugated systems among biologically active compounds are retinol (vitamin A) and retinal, the latter being a substance responsible for vision.s="">Other examples of highly conjugated systems among biologically active compounds are retinol (vitamin A) and retinal, the latter being a substance responsible for vision."">Other examples of highly conjugated systems among biologically active compounds are retinol (vitamin A) and retinal, the latter being a substance responsible for vision.amples of highly conjugated systems among biologically active compounds are retinol (vitamin A) and retinal, the latter being a substance responsible for vision.ples of highly conjugated systems among biologically active compounds are retinol (vitamin A) and retinal, the latter being a substance responsible for vision.es of highly conjugated systems among biologically active compounds are retinol (vitamin A) and retinal, the latter being a substance responsible for vision.of highly conjugated systems among biologically active compounds are retinol (vitamin A) and retinal, the latter being a substance responsible for vision. highly conjugated systems among biologically active compounds are retinol (vitamin A) and retinal, the latter being a substance responsible for vision.ighly conjugated systems among biologically active compounds are retinol (vitamin A) and retinal, the latter being a substance responsible for vision. biologically active compounds are retinol (vitamin A) and retinal, the latter being a substance responsible for vision.iologically active compounds are retinol (vitamin A) and retinal, the latter being a substance responsible for vision.logically active compounds are retinol (vitamin A) and retinal, the latter being a substance responsible for vision.gically active compounds are retinol (vitamin A) and retinal, the latter being a substance responsible for vision.cally active compounds are retinol (vitamin A) and retinal, the latter being a substance responsible for vision.lly active compounds are retinol (vitamin A) and retinal, the latter being a substance responsible for vision.tive compounds are retinol (vitamin A) and retinal, the latter being a substance responsible for vision.ve compounds are retinol (vitamin A) and retinal, the latter being a substance responsible for vision. compounds are retinol (vitamin A) and retinal, the latter being a substance responsible for vision.pounds are retinol (vitamin A) and retinal, the latter being a substance responsible for vision.unds are retinol (vitamin A) and retinal, the latter being a substance responsible for vision.ds are retinol (vitamin A) and retinal, the latter being a substance responsible for vision.explanation for the higher stability of conjugated dienes can be given in describing molecular orbitals of the conjugated systems by example of 1,3-butadiene, a simplest conjugated diene (Fig. 3.1, a).planation for the higher stability of conjugated dienes can be given in describing molecular orbitals of the conjugated systems by example of 1,3-butadiene, a simplest conjugated diene (Fig. 3.1, a).anation for the higher stability of conjugated dienes can be given in describing molecular orbitals of the conjugated systems by example of 1,3-butadiene, a simplest conjugated diene (Fig. 3.1, a).ation for the higher stability of conjugated dienes can be given in describing molecular orbitals of the conjugated systems by example of 1,3-butadiene, a simplest conjugated diene (Fig. 3.1, a).ion for the higher stability of conjugated dienes can be given in describing molecular orbitals of the conjugated systems by example of 1,3-butadiene, a simplest conjugated diene (Fig. 3.1, a).n for the higher stability of conjugated dienes can be given in describing molecular orbitals of the conjugated systems by example of 1,3-butadiene, a simplest conjugated diene (Fig. 3.1, a).for the higher stability of conjugated dienes can be given in describing molecular orbitals of the conjugated systems by example of 1,3-butadiene, a simplest conjugated diene (Fig. 3.1, a).r the higher stability of conjugated dienes can be given in describing molecular orbitals of the conjugated systems by example of 1,3-butadiene, a simplest conjugated diene (Fig. 3.1, a).higher stability of conjugated dienes can be given in describing molecular orbitals of the conjugated systems by example of 1,3-butadiene, a simplest conjugated diene (Fig. 3.1, a).gher stability of conjugated dienes can be given in describing molecular orbitals of the conjugated systems by example of 1,3-butadiene, a simplest conjugated diene (Fig. 3.1, a).er stability of conjugated dienes can be given in describing molecular orbitals of the conjugated systems by example of 1,3-butadiene, a simplest conjugated diene (Fig. 3.1, a).tability of conjugated dienes can be given in describing molecular orbitals of the conjugated systems by example of 1,3-butadiene, a simplest conjugated diene (Fig. 3.1, a).bility of conjugated dienes can be given in describing molecular orbitals of the conjugated systems by example of 1,3-butadiene, a simplest conjugated diene (Fig. 3.1, a).lity of conjugated dienes can be given in describing molecular orbitals of the conjugated systems by example of 1,3-butadiene, a simplest conjugated diene (Fig. 3.1, a).tion">

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return-to-book">turn-to-book">rn-to-book">-to-book">book">ok">37.html.htmltml">Fundamentals of bioorganic chemistryy

Table of contents

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">ivclassasssd="aTCont-ISBN9785970434437-0000nt-ISBN9785970434437-0000-ISBN9785970434437-0000N9785970434437-0000785970434437-00005970434437-0000/ISBN9785970434437-0000.htmlSBN9785970434437-0000.htmlN9785970434437-0000.html5970434437-0000.html70434437-0000.html434437-0000.html-row-doc-aow-doc-a-doc-aasss="aTCont-row-docCont-row-docnt-row-dochrefeflassTCont-row-doc-aont-row-doc-at-row-doc-aTIVITY OF ORGANIC COMPOUNDS.

Chapter 1. CHEMICAL STRUCTURE AND BONDINGVITY OF ORGANIC COMPOUNDS.

Chapter 1. CHEMICAL STRUCTURE AND BONDINGTY OF ORGANIC COMPOUNDS.

Chapter 1. CHEMICAL STRUCTURE AND BONDINGF ORGANIC COMPOUNDS.

Chapter 1. CHEMICAL STRUCTURE AND BONDINGORGANIC COMPOUNDS.

Chapter 1. CHEMICAL STRUCTURE AND BONDINGGANIC COMPOUNDS.

Chapter 1. CHEMICAL STRUCTURE AND BONDINGUCTURE AND BONDINGTURE AND BONDINGRE AND BONDING BONDINGONDINGDINGCont-row-docnt-row-doc-row-docow-doc-docochrefeftps://prior.studentlibrary.ru/en/doc/ISBN9785970434437-0002.htmls://prior.studentlibrary.ru/en/doc/ISBN9785970434437-0002.html//prior.studentlibrary.ru/en/doc/ISBN9785970434437-0002.html="aTCont-row-doc-aCont-row-doc-a-row-doc-aow-doc-aoc-a-aDS"aTCont-ISBN9785970434437-0003Cont-ISBN9785970434437-0003f="https://prior.studentlibrary.ru/en/doc/ISBN9785970434437-0003.htmltps://prior.studentlibrary.ru/en/doc/ISBN9785970434437-0003.htmls://prior.studentlibrary.ru/en/doc/ISBN9785970434437-0003.html//prior.studentlibrary.ru/en/doc/ISBN9785970434437-0003.html3.htmlhtmlmlclassasss STRUCTURE OF ORGANIC MOLECULESTRUCTURE OF ORGANIC MOLECULESUCTURE OF ORGANIC MOLECULESTURE OF ORGANIC MOLECULES OF ORGANIC MOLECULESF ORGANIC MOLECULESGANIC MOLECULESNIC MOLECULESC MOLECULESont-ISBN9785970434437-0004t-ISBN9785970434437-0004ISBN9785970434437-0004efps://prior.studentlibrary.ru/en/doc/ISBN9785970434437-0004.html://prior.studentlibrary.ru/en/doc/ISBN9785970434437-0004.html/prior.studentlibrary.ru/en/doc/ISBN9785970434437-0004.htmlN9785970434437-0004.html785970434437-0004.html5970434437-0004.html70434437-0004.html434437-0004.html4437-0004.html37-0004.htmlter 4. A BRIEF SURVEY OF ORGANIC REACTIONSr 4. A BRIEF SURVEY OF ORGANIC REACTIONS4. A BRIEF SURVEY OF ORGANIC REACTIONS A BRIEF SURVEY OF ORGANIC REACTIONSIEF SURVEY OF ORGANIC REACTIONSF SURVEY OF ORGANIC REACTIONSSURVEY OF ORGANIC REACTIONSrow-docw-docdocc idTCont-ISBN9785970434437-0005tlibrary.ru/en/doc/ISBN9785970434437-0005.htmlibrary.ru/en/doc/ISBN9785970434437-0005.htmlrary.ru/en/doc/ISBN9785970434437-0005.html.ru/en/doc/ISBN9785970434437-0005.htmlu/en/doc/ISBN9785970434437-0005.htmlen/doc/ISBN9785970434437-0005.htmlasss=Cont-row-doc-ant-row-doc-a-row-doc-aICITY OF ORGANIC COMPOUNDSITY OF ORGANIC COMPOUNDSY OF ORGANIC COMPOUNDSOF ORGANIC COMPOUNDS ORGANIC COMPOUNDSRGANIC COMPOUNDSANIC COMPOUNDS TCont-row-doct-row-docrow-doc/en/doc/ISBN9785970434437-0006.htmlen/doc/ISBN9785970434437-0006.html"pter 9. CARBOXYLIC ACIDS AND THEIR DERIVATIVESer 9. CARBOXYLIC ACIDS AND THEIR DERIVATIVES 9. CARBOXYLIC ACIDS AND THEIR DERIVATIVES. CARBOXYLIC ACIDS AND THEIR DERIVATIVESBOXYLIC ACIDS AND THEIR DERIVATIVESXYLIC ACIDS AND THEIR DERIVATIVESLIC ACIDS AND THEIR DERIVATIVES7-0010001010a"PART 3. POLY- AND HETEROFUNCTIONAL COMPOUNDS IN LIVING SYSTEMS. Chapter 10. STEREOISOMERISMRT 3. POLY- AND HETEROFUNCTIONAL COMPOUNDS IN LIVING SYSTEMS. Chapter 10. STEREOISOMERISMPOLY- AND HETEROFUNCTIONAL COMPOUNDS IN LIVING SYSTEMS. Chapter 10. STEREOISOMERISMLY- AND HETEROFUNCTIONAL COMPOUNDS IN LIVING SYSTEMS. Chapter 10. STEREOISOMERISM- AND HETEROFUNCTIONAL COMPOUNDS IN LIVING SYSTEMS. Chapter 10. STEREOISOMERISMNAL COMPOUNDS IN LIVING SYSTEMS. Chapter 10. STEREOISOMERISML COMPOUNDS IN LIVING SYSTEMS. Chapter 10. STEREOISOMERISMCOMPOUNDS IN LIVING SYSTEMS. Chapter 10. STEREOISOMERISMMPOUNDS IN LIVING SYSTEMS. Chapter 10. STEREOISOMERISMNDS IN LIVING SYSTEMS. Chapter 10. STEREOISOMERISMS IN LIVING SYSTEMS. Chapter 10. STEREOISOMERISMIVING SYSTEMS. Chapter 10. STEREOISOMERISMING SYSTEMS. Chapter 10. STEREOISOMERISMG SYSTEMS. Chapter 10. STEREOISOMERISMter 10. STEREOISOMERISMr 10. STEREOISOMERISM10. STEREOISOMERISM STEREOISOMERISMTEREOISOMERISMREOISOMERISMivlass="aTCont-row-docreff=tps://prior.studentlibrary.ru/en/doc/ISBN9785970434437-0011.htmls://prior.studentlibrary.ru/en/doc/ISBN9785970434437-0011.html//prior.studentlibrary.ru/en/doc/ISBN9785970434437-0011.htmlbrary.ru/en/doc/ISBN9785970434437-0011.htmlary.ru/en/doc/ISBN9785970434437-0011.htmly.ru/en/doc/ISBN9785970434437-0011.html785970434437-0011.html5970434437-0011.html70434437-0011.html434437-0011.html4437-0011.html37-0011.html-0011.html1.htmlhtmlml-aChapter 11. POLY- AND HETEROFUNCTIONAL COMPOUNDSapter 11. POLY- AND HETEROFUNCTIONAL COMPOUNDSter 11. POLY- AND HETEROFUNCTIONAL COMPOUNDSONAL COMPOUNDSAL COMPOUNDS COMPOUNDSOMPOUNDSPOUNDSUNDSChapter 14. CARBOHYDRATESMERS AND THEIR STRUCTURAL CONSTITUENTS.

Chapter 14. CARBOHYDRATESRS AND THEIR STRUCTURAL CONSTITUENTS.

Chapter 14. CARBOHYDRATES AND THEIR STRUCTURAL CONSTITUENTS.

Chapter 14. CARBOHYDRATESND THEIR STRUCTURAL CONSTITUENTS.

Chapter 14. CARBOHYDRATES THEIR STRUCTURAL CONSTITUENTS.

Chapter 14. CARBOHYDRATESHEIR STRUCTURAL CONSTITUENTS.

Chapter 14. CARBOHYDRATES STRUCTURAL CONSTITUENTS.

Chapter 14. CARBOHYDRATESTRUCTURAL CONSTITUENTS.

Chapter 14. CARBOHYDRATESUCTURAL CONSTITUENTS.

Chapter 14. CARBOHYDRATESRAL CONSTITUENTS.

Chapter 14. CARBOHYDRATESL CONSTITUENTS.

Chapter 14. CARBOHYDRATESTITUENTS.

Chapter 14. CARBOHYDRATESTUENTS.

Chapter 14. CARBOHYDRATESENTS.

Chapter 14. CARBOHYDRATESr 14. CARBOHYDRATES14. CARBOHYDRATES. CARBOHYDRATESARBOHYDRATESBOHYDRATESHYDRATESivlassssaTCont-row-docCont-row-docnt-row-doc="https://prior.studentlibrary.ru/en/doc/ISBN9785970434437-0015.html//prior.studentlibrary.ru/en/doc/ISBN9785970434437-0015.htmlprior.studentlibrary.ru/en/doc/ISBN9785970434437-0015.htmlior.studentlibrary.ru/en/doc/ISBN9785970434437-0015.htmly.ru/en/doc/ISBN9785970434437-0015.htmlru/en/doc/ISBN9785970434437-0015.html/en/doc/ISBN9785970434437-0015.html001616reff=https://prior.studentlibrary.ru/en/doc/ISBN9785970434437-0016.htmltps://prior.studentlibrary.ru/en/doc/ISBN9785970434437-0016.htmlprior.studentlibrary.ru/en/doc/ISBN9785970434437-0016.htmlior.studentlibrary.ru/en/doc/ISBN9785970434437-0016.htmlr.studentlibrary.ru/en/doc/ISBN9785970434437-0016.htmly.ru/en/doc/ISBN9785970434437-0016.htmlru/en/doc/ISBN9785970434437-0016.html/en/doc/ISBN9785970434437-0016.html/doc/ISBN9785970434437-0016.htmloc/ISBN9785970434437-0016.html/ISBN9785970434437-0016.htmllassssCont-row-doc-ant-row-doc-a-row-doc-aDSasss=prior.studentlibrary.ru/en/doc/ISBN9785970434437-0017.htmlior.studentlibrary.ru/en/doc/ISBN9785970434437-0017.htmlr.studentlibrary.ru/en/doc/ISBN9785970434437-0017.htmlstudentlibrary.ru/en/doc/ISBN9785970434437-0017.htmludentlibrary.ru/en/doc/ISBN9785970434437-0017.htmlentlibrary.ru/en/doc/ISBN9785970434437-0017.htmltlibrary.ru/en/doc/ISBN9785970434437-0017.htmlrary.ru/en/doc/ISBN9785970434437-0017.htmlry.ru/en/doc/ISBN9785970434437-0017.html.ru/en/doc/ISBN9785970434437-0017.htmlen/doc/ISBN9785970434437-0017.html/doc/ISBN9785970434437-0017.htmlSBN9785970434437-0017.htmlN9785970434437-0017.html785970434437-0017.html17.html.htmltml>Chapter 17. NUCLEOTIDES AND NUCLEIC ACIDSapter 17. NUCLEOTIDES AND NUCLEIC ACIDSter 17. NUCLEOTIDES AND NUCLEIC ACIDSr 17. NUCLEOTIDES AND NUCLEIC ACIDS17. NUCLEOTIDES AND NUCLEIC ACIDSUCLEOTIDES AND NUCLEIC ACIDSLEOTIDES AND NUCLEIC ACIDSOTIDES AND NUCLEIC ACIDS-row-docow-doc-docd9785970434437-001885970434437-0018970434437-0018TCont-row-doc-aont-row-doc-at-row-doc-arow-doc-adoc-ac-aa>Appendix 1. Principal Parameters of Covalent Bondsix 1. Principal Parameters of Covalent Bonds 1. Principal Parameters of Covalent Bonds. Principal Parameters of Covalent Bondsameters of Covalent Bondseters of Covalent Bondsers of Covalent Bonds of Covalent Bondsf Covalent BondsCovalent Bondsivs="reffhttps://prior.studentlibrary.ru/en/doc/ISBN9785970434437-0019.htmltps://prior.studentlibrary.ru/en/doc/ISBN9785970434437-0019.htmls://prior.studentlibrary.ru/en/doc/ISBN9785970434437-0019.htmllibrary.ru/en/doc/ISBN9785970434437-0019.htmlbrary.ru/en/doc/ISBN9785970434437-0019.htmlary.ru/en/doc/ISBN9785970434437-0019.htmlivivlassTCont-row-docdTCont-ISBN9785970434437-0020refttps://prior.studentlibrary.ru/en/doc/ISBN9785970434437-0020.htmllassTCont-row-doc-appendix 3. Answers to problemsrow-docw-docdocc" idTCont-ISBN9785970434437-0021t-ISBN9785970434437-0021ISBN9785970434437-002185970434437-0021970434437-00210434437-0021>

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Sadovnicheskaya Str. 11, bldg. 12, Moscow, Russia

Sales Department of "Student's Consultant" ELS

sale@studentlibrary.ru

+7(495)921-39-07 extension 648, 655

Technical support

support@studentlibrary.ru

+7(495)921-39-07

+7(917)550-49-08

Educational establishments

• Humanities higher education establishments
• Agriculture Higher Educational Establishments
• Classical universities
• Technical Higher Education Establishments
• Medical higher education establishments
• Pedagogical higher education establishments

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