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Solutions for Condensations and Alpha Substitutions of Carbonyl Compounds
(g)
CH
C
C
C
H CH
OO
CH
C
C
H2C C
C
H2C
O
CH
O
C
H2C C
CH
C
C
H2C
O
H
H
H
H
H
H
H
H
H
HH H
same enolate as in (g)
H(h)
60 continued
CH
O
CH
C
C
H2C C
C
H2C
O
CH
O
C
H2C C
H
H
H
H
H
H
61 In order of increasing acidity. The most acidic protons are shown in boldface. (The approximate 
pKa values are shown for comparison.) See Appendix 2 in this manual for a review of acidity.