How many of the following alkyl halides will readily undergo SN 1 reaction mechanism?

Question

How many of the following alkyl halides will readily undergo SN 1 reaction mechanism? (A)  (B)  (C)  (D)

Tardigrade Admin · Accepted Answer

Only benzylic halides (1°, 2°, 3°), allylic halides (1°, 2°, 3°) and tertiary alkyl halides undergo S N 1 mechanism most readily. Benzylic halides: (I), (VI) Allylic halides: (II), (IV) Tertiary alkyl halide: (VIII)

Q. How many of the following alkyl halides will readily undergo $S_{N} 1$ reaction mechanism?

Only benzylic halides $(1^{\circ}, 2^{\circ}, 3^{\circ})$ , allylic halides $(1^{\circ}, 2^{\circ}, 3^{\circ})$ and tertiary alkyl halides undergo $S_{N} 1$ mechanism most readily.
Benzylic halides: (I), (VI)
Allylic halides: (II), (IV)
Tertiary alkyl halide: (VIII)

Q. How many of the following alkyl halides will readily undergo SN​1 reaction mechanism?

Only benzylic halides (1∘,2∘,3∘), allylic halides (1∘,2∘,3∘) and tertiary alkyl halides undergo SN​1 mechanism most readily. Benzylic halides: (I), (VI) Allylic halides: (II), (IV) Tertiary alkyl halide: (VIII)

Q. How many of the following alkyl halides will readily undergo $S_{N} 1$ reaction mechanism?

Only benzylic halides $(1^{\circ}, 2^{\circ}, 3^{\circ})$ , allylic halides $(1^{\circ}, 2^{\circ}, 3^{\circ})$ and tertiary alkyl halides undergo $S_{N} 1$ mechanism most readily.
Benzylic halides: (I), (VI)
Allylic halides: (II), (IV)
Tertiary alkyl halide: (VIII)