1. Which one of the foilowing reagents reacts in a similar fashion with both phenylamine (C,H,NH,) and ethylamine. A) Br (aq) C) conc. HNO, D) cold HNO (aq) 2. Phenylamine (aniline) can be prepared by reducing nitrobenzene with tin and concerntrated hydrochloric acid followed by the addition of alkali and finally steam distillation. The alkali is added to; 8 B) conc.H SO, A) prevent oxidation of phenylamine. B) liberate free phenylamine from solution C) dissolve excess nitro benzene D) dissolve the phenylamine Which one of the following statements best explains why trimethylamine [(CH) N] has a lower boiling point than dimeihyiamine [(CH),NH]? A) (CH) N has a larger relative molecular 3. mass B) (CH) N molecule is symmetrical C) (CH) N cannot hydrogen bond with itself (CH IN molecules have a larger volume
1. Which one of the foilowing reagents reacts in a similar fashion with both phenylamine (C,H,NH,) and ethylamine. A) Br (aq) C) conc. HNO, D) cold HNO (aq) 2. Phenylamine (aniline) can be prepared by reducing nitrobenzene with tin and concerntrated hydrochloric acid followed by the addition of alkali and finally steam distillation. The alkali is added to; 8 B) conc.H SO, A) prevent oxidation of phenylamine. B) liberate free phenylamine from solution C) dissolve excess nitro benzene D) dissolve the phenylamine Which one of the following statements best explains why trimethylamine [(CH) N] has a lower boiling point than dimeihyiamine [(CH),NH]? A) (CH) N has a larger relative molecular 3. mass B) (CH) N molecule is symmetrical C) (CH) N cannot hydrogen bond with itself (CH IN molecules have a larger volume
Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter16: Synthesis Workshop 1
Section: Chapter Questions
Problem 46CTQ
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