front 1 Which of the following is not an alkaloid?
| back 1 B) Mesitylene |
front 2 Sec-Butylamine is the common name of what compound?
| back 2 B) 2- butanamine |
front 3 Identify the correct systematic name for the following compound?
| back 3 C) 3-(diethylamino)cyclohex-3-enol |
front 4 Provide the correct IUPAC name for the following amine?
| back 4 C) 4,N-dimethyl-4-penten-2-amine |
front 5 Identify the correct name for the following structure?
| back 5 A) 5-methyl-4-methylaminocyclohept-5-enol |
front 6 Which of the following is a tertiary amine?
| back 6 D) N,N-dimethylaniline |
front 7 Which of the following is a secondary amine?
| back 7 E) N-ethyl-1-propanamine |
front 8 Which of the following amines is most soluble in water?
| back 8 E) Ethylamine |
front 9 Which of the following compounds is a secondary amine?
| back 9 C) N-ethylaniline |
front 10 Which of the following amines can be resolved into enantiomers?
| back 10 C) 2-pentanamine |
front 11 The Nitrogen atome of trimethylamine is ______ hybridized which is reflected in the CNC bond angle _____
| back 11 E) sp3, 108 |
front 12 The Nitrogen's lone pair in pyrrolidine is best described as occupying which type of orbital?
| back 12 B) Sp3 |
front 13 Which of the following compounds contains a tertiary amine?
| back 13 D) 2 and 4 |
front 14 Why cant N-methyl-2-propanamine be resolved into isolable enantiomers even though the compound is chiral? | back 14 Enantiomers interconvert rapidly vis nitrogen inversion |
front 15 The following structure has been used in monitoring the development of amyloid plaques in Alzheimers patients. Which sequences correctly ranks the following nitrogens in order of increasing Pkb value?
| back 15 A) 2<3<1 |
front 16 Which of the following amines is most basic?
| back 16 D) piperidine |
front 17 Which of the following amines is the strongest base?
| back 17 D) piperidine |
front 18 Physostigmine is used in the treatment of glaucoma. Within this structure, the atom indicated by ______ is most basic, while atom ______ is least basic.
| back 18 A) 1 (most basic), 4 (least basic) |
front 19 In 1H NMR protons on the alpha- Carbon of amines typically absorb between theta.
| back 19 B) 2.0 and 3.0 ppm |
front 20 In the mass spectrum of dipropylamine, the base peak appears at m/z ______
| back 20 C) 72 |
front 21 The alpha- Carbon atome bonded to the Nitrogen of an alkylamine usually appears in what chemical shift range?
| back 21 B) 30-50 |
front 22 A three Carbon, Nitrogen-containing compound exhibits 3 13c NMR peaks ( 11.2, 27.3, 44.9) Which of the following compounds best matches the spectral data?
| back 22 D) Ch3Ch2Ch2Nh2 |
front 23 When pentanal reacts with ethylamine under conditions of acid catalysis, the major organic product is ____
| back 23 C) An imine |
front 24 When Ch3Ch2ChO reacts with PhNhNh2 under conditions of acid catalysis, the major organic product is _____
| back 24 E) a hydrazone |
front 25 When pyrrole undergoes EAS at which position does substitution occur?
| back 25 A) 2- position |
front 26 Which of the following chloropyridines readily undergo NAS upon treatment with NaCN?
| back 26 D) Both A and C |
front 27 Pyridine typically undergoes EAS _____ rapidly than benzene, and its preferred site of substitution is the ________ - position
| back 27 E) Less, 3 |
front 28 When pyridine is treated with a mixture of Nitric and Sulfuric acids, the major product is:
| back 28 B) 3-nitropyridine |
front 29 Which compound would react most rapidly with sodium methoxide and heat?
| back 29 B) 2-chloropyridine |
front 30 Which compound results from the reaction below?
| back 30 D) quaternary ammonium salt |
front 31 When a Primary amine reacts with an alkyl sulfonyl chloride, the major organic product is ______
| back 31 E) A sulfonamide |
front 32 The Hofmann eliminations proceeds via a ______ pathway?
| back 32 A) E2 |
front 33 Heating a(n)_____ results in Cope elimination
| back 33 A) amine oxide |
front 34 Secondary amines react with the nitrosonium ion to generate:
| back 34 C) N-nitrosoamines |
front 35 Which of the following amines could be formed by reduction of an amide?
| back 35 C) 1 and 4 |
front 36 Which of the following would be the best phase transfer catalyst?
| back 36 B) N((Ch2)5Ch3)4I |