Tertiary alkyl halides, R 3 CX, undergo spontaneous dissociation to yield a carbocation, R 3 C , plus halide ion Which do you think reacts faster, (CH 3 ) 3 CBr or H 2 C CHC (CH 3 ) 2 Br Explain ...

As we saw tertiary carbocations R 3 C are more stable than either secondary or prim ...

Tertiary alkyl halides, R 3 CX, undergo spontaneous dissociation to yield a carbocation, R 3 C +

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Tertiary alkyl halides, R₃CX, undergo spontaneous dissociation to yield a carbocation, R₃C⁺, plus halide ion. Which do you think reacts faster, (CH₃)₃CBr or H₂C = CHC (CH₃)₂Br? Explain.

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Organic Chemistry

ISBN: 9780495112587

7 Edition

Authors: John McMurry

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Question Posted: Mar 04, 2011 05:26 AM

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Tertiary alkyl halides, R 3 CX, undergo spontaneous dissociation to yield a carbocation, R 3 C +

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Organic Chemistry

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