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(c) Describe by writing an equation how can ethanamide be prepared in the lab?
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(d) How can we prepare a substituted amide in the lab? Write an equation for the formation
of N-ethylethanamide.
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(e) What would you observe in both of the above reactions?
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2 Unlike amines amides are not bases. Solutions of amides are neutral.
(a) Explain the above statement.
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(b) How are amides hydrolyzed? State the possible reagents and conditions
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(c) Describe the acid hydrolysis of ethanamide and write an equation for the reaction
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(d) Write a general equation for this reaction
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(e) Describe the alkaline hydrolysis of ethanamide and write an equation for the reaction
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(f) How can the carboxylic acid be liberated from the product formed in (e)?
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(g) Write an equation for the alkaline hydrolysis of N-ethylethanamide
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(h) How can you obtain a carboxylic acid from the product in the above reaction?
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(i)
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All amino acids except 2- amino ethanoic acid contain an asymmetric carbon atom. What kind of
isomerism are they likely to show ? Using the general formula of a 2- amino carboxylic acid show
how they exhibit this type of isomerism?
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12
What is the physical state of amino acids at room temperature and pressure? Comment on the
melting points and solubility of amino acids
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13 Amino acid solutions resist any changes in pH when small amounts of acid or alkali are added to
them. What are such solutions called?
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(i)
(ii)
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Show the three forms in which amino acids may exist depending on the pH of the solution
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