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>> No.6660010 [View]
File: 75 KB, 600x700, 1358494775904.jpg [View same] [iqdb] [saucenao] [google]
6660010

Any chemists here?

Why can alkyllithium compounds react with carboxylic acids to form ketones, when Grignard reagents will just give an acid-base reaction? And why isn't the product a tertiary alcohol, like when reacting with esters?

>> No.6660009 [DELETED]  [View]
File: 75 KB, 600x700, 1358494775904.jpg [View same] [iqdb] [saucenao] [google]
6660009

Any chemists here?

Why can alkyllithium compounds react with carboxylic acids to form ketones, when Grignard reagents will just give an acid-base reaction? And why isn't the product a tertiary alcohol, like when reacting with esters?

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