Explain acetone attack the carbonyl of cinnamaldehyde

Reference no: EM13517055

Why does the enolate of acetone attack the carbonyl of cinnamaldehyde rather than the carbonly of another acetone molecule?

Starting with a racemic mixture of 2-bromohexanoic acid, one expects a racemic mixture of norleucine. If one started with (S) 2- bromohexanoic acid, would the final product be R or S or racemic?

Why is it necessary to perform solubility test at different pHs?

Would a reaction be faster or slower if a solvent less polar than water were used? Explain

Reference no: EM13517055

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Explain acetone attack the carbonyl of cinnamaldehyde : Why does the enolate of acetone attack the carbonyl of cinnamaldehyde rather than the carbonly of another acetone molecule

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