Which of the following will be most reactive for $S_{N} 1$ reaction?

(C H_{3})_{3} C - C l

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(C H_{3})_{2} C H - C l

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(C H_{3})_{2} N - C H_{2} C l

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(C H_{3})_{3} C - B r

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Solution

The correct option is A $(C H_{3})_{3} C - C l$
Solution
Alkyl group are electron giving groups therefore it stabilises the Positive charge of C atom to which halide is connected.
Therefore that compound become most reactive
Hence Option A and B are more reactive than B,C because A,B have 3 alkyl groups present .
Among A and B , Option A is more reactive because it has more electronegative halide than option B
The correct option is A

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Similar questions

Which of the following alkyl halides will undergo $S_{N} 1$ reaction most readily?

(a) $(C H_{3})_{3} C - F$ (b) $(C H_{3})_{3} C - C l$ (c) $(C H_{3})_{3} C - B r$ (d) $(C H_{3})_{3} C - I$

The arrangement of $(C H_{3})_{3} C -, (C H_{3})_{2} C H -, C H_{3} C H_{2} -$ When attached to a benzene or an unsaturated group in increasing order of inductive effect is:

Q. Major product of the reaction,

(C H_{3})_{3} C - C l + C_{2} H_{5} O N a \to

would be:

The correct order of stability of the following carbanions is:

$(C H_{3})_{3} C^{-},^{-} C C l_{3}, (C H_{3})_{2} C H^{-}, C_{6} H_{5} - C H_{2}^{-}$

Q. Which of the following compound will be most reactive for

S_{N} 1

reactions?

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Which of the following will be most reactive for SN1 reaction?

Which of the following will be most reactive for $S_{N} 1$ reaction?