1
Q
Aza anolate are
A
Strong nucleophile
Strong base
So w obtain 2 products
Aza enolae + alpha halogenation carbonyl derivatives = sn2+ e2 elimination
2
Q
Weak nucleophile are derivatives of
A
Enols
3
Q
If alkylation of tertiary halide made then which mechanism it will follow
A
SN1 MECHANISM
Weak nucleophile is used ( tertiary alkyl halide, benzyl,allyl)
Substrate ( enolate of silly methyl)
4
Q
Lecture 10 …54
A
Name Reaction
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