16.46 Rank the following compounds in order of increasing reactivity in electrophilic bromination. In each case, indi- cate whether the principal monobromination products will be the ortho and para isomers or the meta isomer, and whether the compound will be more or less reactive than benzene. Explain carefully the points that cause any uncertainty. -N(CH3)3 deact CH,N(CH3)3 A meta B N(CH3), CH3 IS.

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s on
16.46 Rank the following compounds in order of increasing
reactivity in electrophilic bromination. In each case, indi-
cate whether the principal monobromination products
will be the ortho and para isomers or the meta isomer,
and whether the compound will be more or less reactive
than benzene. Explain carefully the points that cause any
uncertainty.
the
ху-
the
nan
-CH,N(CH,),
N(CH3)3
deact
A meta
В
ng
agents.
N(CH,),
CH3
act
act
ol P
D
Transcribed Image Text:s on 16.46 Rank the following compounds in order of increasing reactivity in electrophilic bromination. In each case, indi- cate whether the principal monobromination products will be the ortho and para isomers or the meta isomer, and whether the compound will be more or less reactive than benzene. Explain carefully the points that cause any uncertainty. the ху- the nan -CH,N(CH,), N(CH3)3 deact A meta В ng agents. N(CH,), CH3 act act ol P D
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Applying inductive, hyperconjugation & mesomeric effect .

Mesomeric >hyperconjugation> inductive effect

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