3. Show the mechanism for the acid catalyzed addition of H2O to the following ketone. OH H20 CH3 H*

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3. Show the mechanism for the acid catalyzed addition of H2O to the following ketone.
OH
H20
CH3
H*
4. The scheme below shows the reaction of a ketone, 2-propanone with methanol.
OH
:0 :
||
CH,-C-CH3
: ОН
+ H
CH,
c-CH3
CH;-C-CH3
N
step 1
step 2
step 3
P
CH,OH
CH3
CH,OH
step 4
+ H
OCH3
CH,-C-CH3
H
- H,0
C-CH3
ÓCH,
S
CH;
step 7
step 6
step 5
OCH3
i) Write the missing structures (N, O, Q and R) in the above reaction scheme.
ii) Name the class of compounds P and S belong to?
iii) This is an acid catalyzed reaction. What does this statement mean?
iv) Draw the arrow diagram in step 6 to show how intermediate R is formed? Write the
equation for this step ONLY.
v) Steps 3 and 7 involve loss of a proton from the intermediate ions. Why is this step
necessary?
Transcribed Image Text:3. Show the mechanism for the acid catalyzed addition of H2O to the following ketone. OH H20 CH3 H* 4. The scheme below shows the reaction of a ketone, 2-propanone with methanol. OH :0 : || CH,-C-CH3 : ОН + H CH, c-CH3 CH;-C-CH3 N step 1 step 2 step 3 P CH,OH CH3 CH,OH step 4 + H OCH3 CH,-C-CH3 H - H,0 C-CH3 ÓCH, S CH; step 7 step 6 step 5 OCH3 i) Write the missing structures (N, O, Q and R) in the above reaction scheme. ii) Name the class of compounds P and S belong to? iii) This is an acid catalyzed reaction. What does this statement mean? iv) Draw the arrow diagram in step 6 to show how intermediate R is formed? Write the equation for this step ONLY. v) Steps 3 and 7 involve loss of a proton from the intermediate ions. Why is this step necessary?
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