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Q.

Which of the following statements is not correct?

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a

In SN1 mechanism, the rate determining step involves only one molecule.

b

In SN1 mechanism, intramolecular arrangement is possible.

c

In chiral molecule, the SN1 mechanism produces racemic mixture.

d

The intermediate formed in SN1 mechanisms involves five atoms attached to carbon centre of substitution reaction.

answer is D.

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Detailed Solution

(1) SN1 reaction: Take into account tert-butyl bromide's alkaline hydrolysis to produce tert-butanol.
CH3CCH32Br+NaOHΔCH3CCH32OH+NaBr
Only the concentration of tert-butyl bromide affects the pace of the reaction; the hydroxide ion concentration has no effect.
Rate is equal to =KCH3CCH32Br
The reaction happens in this order: 1. Breaking of the carbon-Br bond is followed by the creation of the carbon-hydroxide ion bond in the rate-determining step. As only tert-butyl bromide is involved in the step that determines reaction rate, the reaction is hence unimolecular.

SN1 is a single-molecular nucleophilic substitution process as a result.

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