M Moka11 Full Member 10+ Year Member Apr 25, 2013 #1 Advertisement - Members don't see this ad For Chlorination of a Cyclohexanone: Being that the carbonyl group is electron withdrawing doesnt that make the Chloride add to the meta carbon? (In the roadmap its Ortho under acidic conditions.)
Advertisement - Members don't see this ad For Chlorination of a Cyclohexanone: Being that the carbonyl group is electron withdrawing doesnt that make the Chloride add to the meta carbon? (In the roadmap its Ortho under acidic conditions.)
K KyoPhan Full Member 10+ Year Member 15+ Year Member Apr 25, 2013 #2 The ortho/meta/para directing group only applies to aromatic rings; and you shouldn't see a C=O in an aromatic ring. Upvote 0 Downvote
The ortho/meta/para directing group only applies to aromatic rings; and you shouldn't see a C=O in an aromatic ring.
M Moka11 Full Member 10+ Year Member Apr 25, 2013 #3 KyoPhan said: The ortho/meta/para directing group only applies to aromatic rings; and you shouldn't see a C=O in an aromatic ring. Click to expand... O man my bad, thanks. I think what I was seeing was Alpha Halogenation. Upvote 0 Downvote
KyoPhan said: The ortho/meta/para directing group only applies to aromatic rings; and you shouldn't see a C=O in an aromatic ring. Click to expand... O man my bad, thanks. I think what I was seeing was Alpha Halogenation.
Imazergling Membership Revoked Removed 10+ Year Member Apr 25, 2013 #4 KyoPhan said: The ortho/meta/para directing group only applies to aromatic rings; and you shouldn't see a C=O in an aromatic ring. Click to expand... yes. PREACH Upvote 0 Downvote
KyoPhan said: The ortho/meta/para directing group only applies to aromatic rings; and you shouldn't see a C=O in an aromatic ring. Click to expand... yes. PREACH
