Of trans

According to Kramers model, for flat barrier tops associated with predominantly small barriers, the transition from the low- to the high-damping regime is expected to occur in low-density fluids. This expectation is home out by an extensively studied model reaction, the photoisomerization of tran.s-stilbene and similar compounds [70, 71] involving a small energy barrier in the first excited singlet state whose decay after photoexcitation is directly related to the rate coefficient of tran.s-c/.s-photoisomerization and can be conveniently measured by ultrafast laser spectroscopic teclmiques. 

Figure A3.6.9. Viscosity dependence of photoisomerization rate constants of tran.s -stilbene (open circles) and E,E-diphenylbutadiene (fiill circles) in n-butanol. The broken line indicates a -dependence of k [96],...

Figure A3.6.10. Viscosity dependence of photoisoinerization rate constants of tran.s-stilbene (open circles)...

Schroeder J, Schwarzer D, Troe J and Voss F 1990 Cluster and barrier effects in the temperature and pressure dependence of the photoisomerization of trans.stilbene J. Chem. Phys. 93 2393-404... 

Sundstrdm V and Gillbro T 1984 Dynamics of the isomerization of trans-stiibene in n-alcohols studied by ultraviolet picosecond absorption recovery Chem. Phys. Lett. 109 538-43... 

Sundstrdm V and Gillbro T 1985 Dynamics of trans-cis photoisomerization of stiibene in hydrocarbon solutions Ber. Bunsenges Phys. Chem. 89 222-6... 

Schroeder J 1997 Picosecond kinetics of trans-cis photoisomerisations from ]et-cooled molecules to compressed solutions Ber. Bunsenges Phys. Chem. 101 643... 

Freunscht P, Van Duyne R P and Schneider S 1997 Surface-enhanced Raman spectroscopy of trans-stilbene adsorbed on platinum- or self-assembled monolayer-modified silver film over nanosphere surfaces Chem. Phys. Lett. 281 372-8... 

Yang W H, Hulteen J 0, Schatz G G and Van Duyne R P 1996 A surface-enhanced hyper-Raman and surface-enhanced Raman scattering study of trans-1,2-bis(4-pyridyl)ethylene adsorbed onto silver film over nanosphere electrodes. Vibrational assignments experiments and theory J. Chem. Phys. 104 4313-26... 

Lee M, Holtom G R and Hoohstrasser R M 1985 Observation of the Kramers turnover region in the isomerism of trans-stilbene in fluid ethane Chem. Phys. Lett. 118 359-63... 

TlypcrC hcin uses the eigenvector I ollowing inelhod described in Bnker, J, An Algorllhin for the Lociillon of Tran sition SLiiics, ... 

With all-atom simulations the locations of the hydrogen atoms are known and so the order parameters can be calculated directly. Another structural property of interest is the ratio of trans conformations to gauche conformations for the CH2—CH2 bonds in the hydrocarbon tail. The trans gauche ratio can be estimated using a variety of experimental techniques such as Raman, infrared and NMR spectroscopy. 

Ketones, in which one alkyl group R is sterically demanding, only give the trans-enolate on deprotonation with LDA at —12°C (W.A. Kleschick, 1977, see p. 60f.). Ketones also enolize regioseiectively towards the less substituted carbon, and stereoselectively to the trans-enolate, if the enolates are formed by a bulky base and trapped with dialkyl boron triflates, R2BOSO2CF3, at low temperatures (D A. Evans, 1979). Both types of trans-enolates can be applied in stereoselective aldol reactions (see p. 60f.). 

Phenyl-1,4-hcxadicnc (122) is obtained as a major product by the codimerization of butadiene and styrene in the presence of a Lewis acid[110]. Pd(0)-catalyzed addition reaction of butadiene and aiiene (1 2) proceeds at 120 C to give a 3 1 mixture of trans- and c -2-methyl-3-methylene-l,5.7-octatriene (123)[lll]. 

In the carbonylation of trans,trans,cis-CDT, the trans double bond is attacked preferentially to give the monoester 10, and then the diester 11. Attack of the cis double bond to give the triester is slow[15]. Only the C-16 alkene was carbonylated regio- and stereoselectively to give the Ibo-carboxy-late 12 by carbonylation of the C-5 and C-16 unsaturaied steroid[]6]. 

The ultraviolet spectra of these compounds are similar to those of trans stilbene or of 2- and 4-stilbazole. The effect on the ultraviolet spectrum of various substituents have been found to parallel in many respects the efiects produced by the corresponding group in derivatives of aromatic hydrocarbons (142). 

The CIS and trans forms of 1 2 dimethylcyclopropane are stereoisomers Stereoisomers are isomers that have their atoms bonded m the same order—that is they have the same constitution but they differ m the arrangement of atoms m space Stereoiso mers of the cis-trans type are sometimes referred to as geometric isomers You learned m Section 2 18 that constitutional isomers could differ m stability What about stereoisomers We can measure the energy difference between as and trans 1 2 dimethylcyclo propane by comparing their heats of combustion As illustrated m Figure 3 20 the two compounds are isomers and so the difference m their heats of combustion is a direct measure of the difference m their energies Because the heat of combustion of trans 1 2 dimethylcyclopropane is 5 kJ/mol (12 kcal/mol) less than that of its cis stereoisomer it follows that trans 1 2 dimethylcyclopropane is 5 kJ/mol (12 kcal/mol) more stable than as 1 2 dimethylcyclopropane... 

The most stable conformation of trans 1 4 dimethylcyclohexane has both methyl groups in equatorial orientations The two chair conformations of trans 1 4 dimethyl cyclohexane are not equivalent to each other One has two equatorial methyl groups the other two axial methyl groups... 

Both methyl groups are equatorial m the most stable conformation of trans 1 2 dimethyl cyclohexane... 

Most stable conformation of trans 1 3 dimethylcyclohexane (one axial methyl group)... 

In addition to being regioselective alcohol dehydrations are stereoselective A stereo selective reaction is one m which a single starting material can yield two or more stereoisomeric products but gives one of them m greater amounts than any other Alcohol dehydrations tend to produce the more stable stereoisomer of an alkene Dehydration of 3 pentanol for example yields a mixture of trans 2 pentene and cis 2 pentene m which the more stable trans stereoisomer predominates... 

Suggest an efficient synthesis of trans 2 heptene from propyne... 

The transition in the UV spectrum of trans stilbene trans C6H5CH=CHCgH5)... 

Construct a molecular model of trans 2 bromocyclohexanol in its most stable conformation This conformation is ill suited to undergo epoxide formation on treatment with base Why2 What must happen in order to produce 1 2 epoxycyclohexane from trans 2 bromocyclohexanoP... 

A few fatty acids with trans double bonds (trans fatty acids) occur naturally but the major source of trans fats comes from partial hydrogenation of vegetable oils m for example the preparation of margarine However the same catalysts that catalyze the... 

When the asymmetric carbon atoms in a chiral compound are part of a ring, the isomerism is more complex than in acyclic compounds. A cyclic compound which has two different asymmetric carbons with different sets of substituent groups attached has a total of 2 = 4 optical isomers an enantiometric pair of cis isomers and an enantiometric pair of trans isomers. However, when the two asymmetric centers have the same set of substituent groups attached, the cis isomer is a meso compound and only the trans isomer is chiral. (See Fig. 1.15.)... 

Infrared spectra of fats and oils are similar regardless of their composition. The principal absorption seen is the carbonyl stretching peak which is virtually identical for all triglyceride oils. The most common appHcation of infrared spectroscopy is the determination of trans fatty acids occurring in a partially hydrogenated fat (58,59). Absorption at 965 - 975 cm is unique to the trans functionaHty. Near infrared spectroscopy has been utilized for simultaneous quantitation of fat, protein, and moisture in grain samples (60). The technique has also been reported to be useful for instmmental determination of iodine value (61). 

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