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SN1 Reaction Mechanism

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what happen when (+)2- iodobutane is treated with NaI in dry acetone??SINCE THIS REACTION FOLLOW SN2 MECHANISM THEN WHY RACEMIC MIXTURE IS FORMED (WHICH IS PROPERT OF SN1)

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Q. Assertion :Optically active

2

-iodobutane on treatment with

N a I

in acetone undergoes racemization.
Because Reason: Repeated Walden inversions on the reactant and its product eventually give a racemic mixture.

Assertion : Optically active 2-iodobutane on treatment with NaI in acetone undergoes recemization.

Reason : Repeated Walden inversions on the reactant and its product eventually gives a racemic mixture.

Q. When a chiral alkyl halide undergoes a

S_{N} 1

reaction, a racemic mixture is formed.

Q. (R)-2 -Iodobutane is treated with NaI in acetone and allowed to stand for a long time.The product eventually formed is:

Q. Which one of the following compounds will give racemic mixture in

S_{N} 1

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