Identify the false statement regarding chiral | vedclass

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Question

(C) Step $1$: Enantiomers are non-superimposable mirror images of each other. Therefore, the statement in option $(C)$ is false.Step $2$: $S_N1$ react

Vedclass · Accepted Answer

Enantiomers are superimposable mirror images of each other.

Vedclass · Answer

(C) Step $1$: Enantiomers are non-superimposable mirror images of each other. Therefore, the statement in option $(C)$ is false.Step $2$: $S_N1$ reactions proceed via a carbocation intermediate, leading to racemization ($1$:$1$ mixture of enantiomers).Step $3$: $A$ racemic mixture contains equal amounts of two enantiomers, resulting in zero net optical rotation.Step $4$: $S_N2$ reactions involve a backside attack, resulting in the Walden inversion of configuration.

Identify the false statement regarding chirality from the following.

Similar Questions

Select the incorrect option:

The decreasing order of the rate of $S_{N^1}$ reaction for the following compounds is:
$I$. $Ph-C(Br)(CH_3)-Ph$
$II$. $Ph-CH(Br)-Ph$
$III$. $Ph-CH(Br)-CH_3$
$IV$. $Ph-CH_2Br$

Identify the major product for the following reaction:
$1$-fluoro-$1$-methylcyclohexane $\xrightarrow[\Delta]{Alc. KOH}$ ?

Which of the following statements is correct regarding the rate of hydrolysis of the compounds $(A)$ and $(B)$ by $S_N1$ reaction?

Identify the major product $(P)$ in the following reaction sequence.
$(CH_3)_3 CBr$ $\xrightarrow{\text{Alcoholic } KOH, \Delta}$ $\xrightarrow{HBr} P$

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