Provide the structure and name of the aldehyde with the formula, C2H4O. (b) Draw the two steps of the Strecker synthesis used for the conversion of the aldehyde in part (a) into racemic alanine. (c) Draw the (R) and (S) enantiomers of alanine. Which is the naturally occurring enantiomer? (d) Draw the structure of the dipeptide, Ala-Gly.

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Answer ALL parts of this question.
(a) Provide the structure and name of the aldehyde with the formula, C2H4O.
(b) Draw the two steps of the Strecker synthesis used for the conversion of the
aldehyde in part (a) into racemic alanine.
(c) Draw the (R) and (S) enantiomers of alanine. Which is the naturally occurring
enantiomer?
(d) Draw the structure of the dipeptide, Ala-Gly.
Transcribed Image Text:Answer ALL parts of this question. (a) Provide the structure and name of the aldehyde with the formula, C2H4O. (b) Draw the two steps of the Strecker synthesis used for the conversion of the aldehyde in part (a) into racemic alanine. (c) Draw the (R) and (S) enantiomers of alanine. Which is the naturally occurring enantiomer? (d) Draw the structure of the dipeptide, Ala-Gly.
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