Y yoh95 Full Member 7+ Year Member Joined Jun 16, 2014 Messages 91 Reaction score 7 Jul 20, 2017 #1 Will it be the aldehyde since it is more reactive? Members don't see this ad.
spdental Full Member 5+ Year Member Joined May 19, 2017 Messages 202 Reaction score 135 Jul 20, 2017 #2 Aldehyde because less steric repulsion (H vs a CH3). Upvote 0 Downvote
D deleted853480 Jul 20, 2017 #3 Most likely the aldehyde. But is the aldehyde has a really bulky R group like t butyl then it could go ketone. Upvote 0 Downvote
Most likely the aldehyde. But is the aldehyde has a really bulky R group like t butyl then it could go ketone.
W Wererew Full Member 5+ Year Member Joined Jun 1, 2017 Messages 106 Reaction score 27 Jul 20, 2017 #4 Yes Upvote 0 Downvote
Y yoh95 Full Member 7+ Year Member Joined Jun 16, 2014 Messages 91 Reaction score 7 Jul 20, 2017 #5 spdental said: Aldehyde because less steric repulsion (H vs a CH3). Click to expand... Mr Donald Mouse said: Most likely the aldehyde. But is the aldehyde has a really bulky R group like t butyl then it could go ketone. Click to expand... Wererew said: Yes Click to expand... Thank you! Upvote 0 Downvote
spdental said: Aldehyde because less steric repulsion (H vs a CH3). Click to expand... Mr Donald Mouse said: Most likely the aldehyde. But is the aldehyde has a really bulky R group like t butyl then it could go ketone. Click to expand... Wererew said: Yes Click to expand... Thank you!
