Infrared spectra and conformational equilibrium of cis- and trans-2-chloromethylcyclohexanes

1973 ◽  
Vol 19 (4) ◽  
pp. 1369-1371
Author(s):  
U. Kh. Agaev ◽  
A. T. Alyev ◽  
S. Z. Rizaeva ◽  
Yu. A. Pentin
1968 ◽  
Vol 46 (1) ◽  
pp. 21-24 ◽  
Author(s):  
W. W. Zajac Jr. ◽  
F. Sweet ◽  
R. K. Brown

Infrared spectra show both free and hydrogen bonded hydroxyl absorption in several trans-2-alkoxy-3-hydroxytetrahydrofurans. The extent of non-bonded hydroxyl is greater than that of bonded hydroxyl. Suggestions are made of possible conformations which might account for the infrared data.


1952 ◽  
Vol 30 (12) ◽  
pp. 963-972 ◽  
Author(s):  
H. J. Bernstein ◽  
A. D. E. Pullin

The infrared spectra of the vapor and the liquid, and the Raman spectra of liquid cis and trans C2HDCl2 have been obtained in the region 400–3300 cm−1 The observed spectra are in accordance with the assignment of Bernstein and Ramsay for cis and trans C2H2Cl2 and C2D2Cl2.


1998 ◽  
Vol 109 (1) ◽  
pp. 177-185 ◽  
Author(s):  
Lester Andrews ◽  
Mingfei Zhou ◽  
Stephen P. Willson ◽  
Gary P. Kushto ◽  
Anders Snis ◽  
...  

1975 ◽  
Vol 29 (6) ◽  
pp. 501-506 ◽  
Author(s):  
J. E. Katon ◽  
Philip D. Miller

The complete vibrational spectra of α-bromoacetaldehyde dimethyl acetal and α-bromoacetaldehyde dimethyl s6 have been recorded on the pure liquids, and a tentative vibrational assignment has been proposed. The infrared spectra of both compounds in the crystal state have also been recorded at low temperatures. There is no apparent evidence of a conformational equilibrium in the liquid phase. The infrared spectra of three other acetals have been recorded, and the data from all of the compounds are discussed in terms of previously proposed group frequencies of acetals in both the infrared and Raman.


1979 ◽  
Vol 44 (2) ◽  
pp. 410-419 ◽  
Author(s):  
Soňa Vašíčková ◽  
Miloš Tichý

Infrared bands due to carbonyl and hydroxyl stretching vibration were measured for 32 esters of substituted cyclohexane and trans-decalin carboxylic acids and 2-hydroxy acids. The bands were computer-separated and most of them assigned to the appropriate rotamers. The conformational equilibrium in methyl trans-2-hydroxy-cis-4-isopropylcyclohexanecarboxylate was determined using comparison of integrated intensities of the hydroxyl bands of the mobile compound with those of the conformationally biased standards. The OH/COOCH3 vicinal interaction was found to be attractive (about 2.6 kJ mol-1).


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