(a)
Interpretation:
The
Concept Introduction:
Amides are formed by a reaction with a carboxylic acid and an amine which are the
The mechanism for formation of an amide is as follows taking example of propanoic acid and ethylamine:
The hydrolysis of amide so formed can give back the carboxylic acid and amine.
(b)
Interpretation:
The carboxylic acid and amine or ammonia needs to be identified from which each amide be synthesized.
Concept Introduction:
Amides are formed by a reaction with a carboxylic acid and an amine which are the functional groups. This results in the formation of amide bond, in which OH group of carboxylic acid reacts with one of the H in amine group and CO-NH bond is formed. This bond is known as an amide bond.
The mechanism for formation of an amide is as follows taking example of propanoic acid and ethylamine:
The hydrolysis of amide so formed can give back the carboxylic acid and amine.
(c)
Interpretation:
The carboxylic acid and amine or ammonia needs to be identified from which each amide be synthesized.
Concept Introduction:
Amides are formed by a reaction with a carboxylic acid and an amine which are the functional groups. This results in the formation of amide bond, in which OH group of carboxylic acid reacts with one of the H in amine group and CO-NH bond is formed. This bond is known as an amide bond.
The mechanism for formation of an amide is as follows taking example of propanoic acid and ethylamine:
The hydrolysis of amide so formed can give back the carboxylic acid and amine.
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Chapter 19 Solutions
Student Solutions Manual for Bettelheim/Brown/Campbell/Farrell/Torres' Introduction to General, Organic and Biochemistry, 11th
- Draw the enantiomer and diastereomers of the following molecule. Label each type of stereoisomers. Label each chiral center as R or S. HOarrow_forwardWhich diene and dienophile would you choose to synthesize the following compound? Please provide a detailed explanation. Please include a drawing showing the mechanism of the synthesis. Please also explain why it is the correct diene and dienophile.arrow_forwardUsing the sketcher below, draw the structure of N-ethyldecylamine. Answer: 0 ୨୫) . 始 {n [ ]t ?arrow_forward
- Which of the following would you expect to be aromatic? Please provide a detailed explanation.arrow_forwardIdentify the characteristic signals that you would expect in the diagnostic region of an IR spectrum of each of the following compounds. a. H₂N b.arrow_forwardWhat is the lowest energy chair for the following cyclohexane? ' || || a. b. " " d.arrow_forward
- Answer the following questions using the below figure: Potential Energy ри Reaction Progress a. How many transition states occur in this reaction? b. How many intermediates occur in this reaction? c. Is this reaction spontaneous or nonspontaneous? d. Does this reaction have a positive or negative AG? e. Label the activation energy(ies).arrow_forwardDraw the following molecule as a chair in the lowest energy conformation. Then perform a chair flip. Brarrow_forwardNonearrow_forward
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