Which of the following compounds can in principle be isolated in optically active form at room temperature?
a. cis-1,4-dimethylcyclohexane
b.trans-1,3-dimethylcyclohexane
c.1,1-dimethylcyclohexane
d.cis-1-ethyl-3-methylcyclohexane
Chiral compounds are optically active and achiral compounds are optically inactive.
The optically compound and its mirror image are not superimposable to each other. It is possible if the compound does not possess any plane of symmetry.
Plane of symmetry is an imaginary plane through which reflection takes place.
The compound which can rotate plane polarized light in clockwise or anti-clockwise direction is known as optically active compound.
The compounds which have plane of symmetry are as follows:
The compounds cis-1,4-dimethylcyclohexane and 1,1-dimethylcyclohexane are achiral compounds and trans-1,3-dimethylcyclohexane and cis-1-ethyl-3-methylcyclohexane are chiral compounds.
Therefore, cis-1,4-dimethylcyclohexane and 1,1-dimethylcyclohexane are optically inactive and trans-1,3-dimethylcyclohexane and cis-1-ethyl-3-methylcyclohexane are optically active.
Hence, trans-1,3-dimethylcyclohexane and cis-1-ethyl-3-methylcyclohexane can be isolated in optically active form.
Ans:The compounds which can be isolated in optically active form at room temperature are as follows:
Which of the following compounds can in principle be isolated in optically active form at room temperature?
Which of the following molecules is chiral at room temperature (25 degree C) and why? A.1,1-dimethylcyclohexane B.cis-1,2-dimethylcyclohexane C.trans-1,3- dimethylcyclohexane D, trans- 1,4 - dimethylcyclohexane
10) Which of the following are optically inactive? A) a 50-50 mixture of Rand Senantiomers B) a racemic mixture C) every achiral compound D) a meso compound E) all the above 11) If (S)-glyceraldehyde has a specific rotation of -8.7, what is the specific rotation of (R)-glyceraldehyde? A) +8.7 B) -8.7 C) 0.0 D) cannot be determined from the information given 12) What is the relationship between the following compounds? HCI CH - CH₂ CH3 HEC HCI HEC X сін...
2.37 Draw the formula for the preferred conformation of a. bromocyclohexane. c. cis-1-ethyl-3-methylcyclohexane. b. trans-1,4-dimethylcyclohexane. d. 1,1-dichlorocyclohexane.
b. Which of the following alkanes has the highest bolling point? 2,3-dimethylbutane: 2-methylpentane; 3-methylpentane; hexane c. Which of the following compounds can adopt a chair conformation in which there are no axial methyl groups? 1,1-dimethylcyclohexane; cis-1,2-dimethylcyclohexane; trans-1,2-dimethylcyclohexane; trans-1,3-di methylcyclohexane d. Which of the following compounds can adopt a chair conformation which there are no axial methyl groups? cis-1,2-dimethylcyclohexane; cis-1,3-dimethylcyclohexane; trans-1,3-dimethylcyclohexane; cis-1.4-dimethylcyclohexane cis-1,2-dimethvcyclohexane (Enter the numerical value only, without any units)? e. What is the approximate di hedral angle between the...
In each of the cases below, which isomer is more stable? a) 1,4-dimethylcyclohexane (cis/trans?): b) 1-bromo-2-methylcyclohexane : (cis/trans?) c) 1,3-diethylcyclohexane (cis/trans?)
Which of the following substances can exist in an optically active form? Draw structures, and locate with an asterisk all chiral centers in each a. 2-methylbutane b. 1,2,3,4-tetrachloropentane
7.66 A mixture contains equal amounts of compounds A-D. a. Which compounds alone are optically active? b. If the mixture was subjected to fractional distillation, how many fractions would be obtained? c. How many of these fractions would be optically active?
5.66 A mixture contains equal amounts of compounds A-D. a. Which compounds alone are optically active? b. If the mixture was subjected to fractional distillation, how many fractions would be obtained? c. How many of these fractions would be optically active?
Draw both chair conformations for each of the following compounds. In each case, identify the more stable chair conformation: (a) Methylcyclohexane (b) trans-1,2-Diisopropylcyclohexane (c) cis-1,3-Diisopropylcyclohexane (d) trans-1,4-Diisopropylcyclohexane
4.51 Draw both chair conformations for each of the following compounds. In each case, identify the more stable chair conformation: (a) Methylcyclohexane (b) trans-1,2-Diisopropylcyclohexane (c) cis-1,3-Diisopropylcyclohexane (d) trans-1,4-Diisopropylcyclohexane