Chapter 3.4, Problem 14P

The product of this reaction is: O CI secondary amide secondary amine primary amide tertiary amide primary amine + 2NH3

Draw the reactions for the following products (any or all) (include all products).

Draw the structure of the following three isomeric amides with chemical formula C6H11NO. Amide #1: (E)-N,N-dimethyl-2-butenamide Amide #2: (Z)-N-methyl-3-pentenamide Amide #3: (Z)-3-hexenamide

Which of the following compounds cannot form hydrogen bonds with wate O CH3-CH2-OH 0 1 CH3-C-OH 0 I CH3-C-0-CH3 O CH3-CH2-CH3 0 O) CH3-CH)-NH2 Question 55 Aniline is a(n) O cyclic amine with only single bonds O tertiary aromatic amine O primary aromatic amine O secondary aromatic amine five carbon amine

Amines in aqueous solutions are less reactive than amines in gaseous solutions. Select one: O True O False

Draw the structures of the products when each of the following amides undergo hydrolysis with NaOH. You may want to reference (Page) Section 18.6 while completing this problem. ▼ CH3 0 CH,—CH,—CH—C—NH, Draw the molecules on the canvas by choosing buttons from the Tools (for bonds and charg www NN [1] Submit Part B Request Answer H 120 EXP CONT + Marvin JS by ChemAxon • & H H 120 EXP CONT C N O S CI Br - PFL O CH₂ CH3 CH3-CH₂-CH₂-C-N-CH₂-CH3 Draw the molecules on the canvas by choosing buttons from the Tools (for bonds and charg Р H C Z O

When cyclohexanone was reacted with an amine A. It the reaction formed an enamine, whichof the following is the most likely identity of amine A?

N-Methylpyrrolidine has a boiling point of 81 °C, and piperidine has a boiling point of 106 °C. Tetrahydropyran has a boiling point of 88 °C, and cyclopentanone has a boiling point of 141 °C. These two isomershave a boiling point difference of 53 °C. Explain why the two oxygen-containing isomers have a much larger boilingpoint difference than the two amine isomers

What is the product of the following neutralization reaction between an amine and an acid, as shown below? H CH3—N—CH₂ - CH3 ammonium bromide O ethylmethylamine bromide ethylmethylamine ethylmethylammonium bromide + HBr →