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Which of the ...

Question

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

A

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

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B

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

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C

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

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D

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

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Solution

The correct option is D ${(C H_{3})}_{3} C - I$
Due to large size, iodide ion have less density of charge so it will be most stable and it will follow reaction most easily.

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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) $(C H_{3})_{3} C - I$

Q. The reaction

(C H_{3})_{3} C - B r \to (C H_{3})_{3} C^{+} + B r^{-}

is an example of:

Q. Which of the following carbocation is most stable?

(C H_{3})_{3} C - C H_{2}^{+}

(C H_{3})_{3} C^{+}

C H_{3} C H_{2} C H_{2}^{+}

C H_{3} C H^{+} C H_{2} C H_{3}

Q. In which of the following alkyl halide is

S N_{2}

mechanism is favored the maximum

Q. IUPAC name of

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

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