Draw Fischer projections for the following substitution reactions and choose the correct option:

The reaction proceeds via $S_{N} 2$ largely

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The reaction is $S_{N} 1$ largely

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The product is a racemic mixture

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The major product is optically active.

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Solution

The correct options are
A
The reaction proceeds via $S_{N} 2$ largely

D
The major product is optically active.

The problem is definitely of $S_{N} 2$ and there will be an inversion of configuration at the stereocenter. So the solution is:

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Similar questions

Draw Fischer projections for the following $S_{N} 2$ substitution reaction:

Q. Select the correct options with respect to the reaction of cis-3-methylcyclopentanol with

P B r_{3}

$S_{N} 1$ solvolysis of 1-(bromomethyl)cyclohex-1-ene in ethanol gives:

Draw Fischer projections for the following substitution reaction:

The substitution reaction of optically active alkyl halides in which attack of nucleophile and detachment of halogen takes place in two different steps and racemic mixture is formed as product is:

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Draw Fischer projections for the following substitution reactions and choose the correct option:

The correct options are A The reaction proceeds via SN2 largely D The major product is optically active. The problem is definitely of SN2 and there will be an inversion of configuration at the stereocenter. So the solution is:

The correct options are
A
The reaction proceeds via $S_{N} 2$ largely

D
The major product is optically active.

The problem is definitely of $S_{N} 2$ and there will be an inversion of configuration at the stereocenter. So the solution is: