Questions from Organic Chemistry

Q: Draw the condensed formula for each of the following compounds.

Draw the condensed formula for each of the following compounds. a. Diethyl methylamine b. 4-Methylpentylamine c. N-Methylaniline d. Triisopropylamine e. Methyl-t-butylamine f. Ethyl hexylamine

Q: The amide bond is stabilized by resonance. Draw the contributing resonance

The amide bond is stabilized by resonance. Draw the contributing resonance forms of the amide bond.

Q: Locate the amine functional group in the structure of lidocaine. Is

Locate the amine functional group in the structure of lidocaine. Is lidocaine a primary, secondary, or tertiary amine?

Q: The structure of saccharin, an artificial sweetener, is shown.

The structure of saccharin, an artificial sweetener, is shown. Circle the amide group.

Q: Complete each of the following by supplying the missing reagents. Draw

Complete each of the following by supplying the missing reagents. Draw the structures of each of the reactants and products. a. N-Methylpropanamide +? −−−−→ propanoic acid +? b. N, N-Dimethylacetamide...

Q: Of what significance is it that lysosomal enzymes have a pH optimum

Of what significance is it that lysosomal enzymes have a pH optimum of 4.8?

Q: Write two equations for the synthesis of each of the following amides

Write two equations for the synthesis of each of the following amides. In one equation, use an acid chloride as a reactant. In the second equation, use an acid anhydride. a. Ethanamide b. N-Propylpent...

Q: Write general equations for the synthesis of a primary, secondary,

Write general equations for the synthesis of a primary, secondary, and tertiary amide.

Q: Draw a dipeptide composed of glycine and alanine. Begin by drawing

Draw a dipeptide composed of glycine and alanine. Begin by drawing glycine with its amino group on the left. Circle the amide bond.

Q: Does glycine have a chiral carbon? Explain your reasoning.

Does glycine have a chiral carbon? Explain your reasoning.