Difference Between SN2 and Addition Elimination.

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Nucleophillic addition-elimination occurs whenever you have carbonyl compound with a good leaving group attached at the alpha position to the carbonyl carbon.
351px-AcylSubstitution.svg.png


An SN2 reaction occurs mainly on primary alkyl halides in which the nucleophile attacks from the opposite side of the leaving group. A 5-bond transition state (thank you joshto) is formed, and degrades immediately donating a pair of electrons to the leaving group.
BromoethaneSN2reaction-small.png
 
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Do addition-elimination reactions only occur in carboxylic acid and derivatives? ie. where there is a double bond oxygen that becomes a positively charged water molecule that wants to leave?

edit: i am not expecting the original people in this thread to respond, but replying so as to not just make new threads 😛
 
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