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The drawing on the right shows that trans-1, 3-dichlorocyclohexane is chiral.
Efforts to resolve this compound fail. why?

(a)The cis and trans isomers rapidly interconvert.
(b)The compound is actually a meso structure.
(c)The chair conformers rapidly interconvert producing a racemic mixture.
(d)Method for resolving alkyl chlorides are not available.

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Important Questions on Hydrocarbons
EASY
Identify the geometrical isomers of the following compounds.

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HARD

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Represent the union of two sets by Venn diagram for each of the following.
is a prime number between and
is an odd number between and

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HARD
Assuming the dipole moment of optically inactive isomer of 2,3 -dibromobutane is 0.8 D and the mole fraction of most stable staggered is 0.8. The approximate value of dipole moment due to less stable staggered form of 2,3 -dibromobutane will be

