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Talk:Acyl chloride

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This is an old revision of this page, as edited by Uhjoebilly (talk | contribs) at 00:33, 1 December 2010 (→‎Radical R Group?: new section). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

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Things to do

  • Mechanism of SOCl2, PCl3, PCl5.
  • Mechanism of DMF
  • Balance equation with cyanuric chloride
  • Check - DIBAH reduces to 1° alcohol? Or aldehyde? Reusch says former, Rosenmund reaction says latter.
  • Draw diagram for FC acylation. Reaction in Friedel-Crafts reaction is not very nice.

--Rifleman 82 (talk) 20:26, 19 February 2009 (UTC)[reply]

Radical R Group?

Does the R group in RCOCl really have to be an "organic radical"? Only one reaction shown on the page (the Appel Reaction) had a radical at all. From what I understand, the beauty of Acid Chlorides is that you can put virtually any R group onto it, allowing addition to any nucleophilic functional group.

An explanation would be appreciated, but if one is not available in a few days, I'll go ahead and remove that part of the opening paragraph. Uhjoebilly (talk) 00:33, 1 December 2010 (UTC)[reply]