Identify the Reagents Needed to Make Isoleucine Using the Strecker

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The Answer is The Strecker synthesis starts with an aldehyde and reacts with ammonia to form an imine. Cyanide then adds to form an -amino nitrile. The nitrile is then hydrolyzed to give a carboxylic acid.

The Strecker synthesis starts with an aldehyde and reacts with ammonia to form an imine. Cyanide then adds to form an <font face= symbol ></font>-amino nitrile. The nitrile is then hydrolyzed to give a carboxylic acid. The R group and hydrogen bonded to the alpha carbon on the amino acid must come from the aldehyde. So, the synthesis will be:

The R group and hydrogen bonded to the alpha carbon on the amino acid must come from the aldehyde. So, the synthesis will be:
The Strecker synthesis starts with an aldehyde and reacts with ammonia to form an imine. Cyanide then adds to form an <font face= symbol ></font>-amino nitrile. The nitrile is then hydrolyzed to give a carboxylic acid. The R group and hydrogen bonded to the alpha carbon on the amino acid must come from the aldehyde. So, the synthesis will be:

Identify the Reagents Needed to Make Isoleucine Using the Strecker

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Identify the Reagents Needed to Make Isoleucine Using the Strecker

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Correct Answer:
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