(5 pts) Provide an acceptable name for each of the following structures. >=6 & C
(3 pts each, unless otherwise noted, 17 pts total) 1-5. Nomenclature: provide an acceptable name for each of the following compounds, but do NOT Google. 1. 2. 3. -CO No HN -CO,H COM 5. (5 pts) Name IUPAC ONLY. i HN-CHE H-C-N(CH)2 (4 pts each, unless otherwise noted, 16 pts total) 6-9. Structures: provide an acceptable structure for: 6. the isobutyl diester of B-bromopimelic acid (5 pts) 7. N-ethyl-B-ethyl-y-valerylactam. 8. benzoic B-chloropropionic anhydride (3 pts) 9. o-bromobenzoyl chloride
(3 pts each, unless otherwise noted, 16 pts total) 1-5. Nomenclature: provide an acceptable name for each of the following molecules, but do NOT Google. 1. 2. 3 H2N CO H H-C-N(CH)2 CO, NA (7 pts) 4. НО. CH3 N H CHE
(3 pts each, unless otherwise noted, 16 pts total) 1-5. Nomenclature: provide an acceptable name for each of the following molecules, but do NOT Google. 1. 2. 3 H2N CO H H-C-N(CH)2 CO, NA (7 pts) 4. НО. CH3 N H CHE
Need help with #5-8
(5 pts each, unless otherwise noted, 19 pts total) 5-8. Structures: provide an acceptable structure for: (4 pts) 5. the sec-butyl monoester of B-bromopimelic acid 6. N-methyl-B-isopropyl-5-valerolactam 7. a-chloropropionic ß-aminobutyric anhydride NH2 Br- 8. ethylisopropylmethylpropylammonium bromide
(3 pts) Provide 2 acceptable names for the molecule below. If you provide a systematic name, include the appropriate R or S designation in the name. (2 pts) Provide a systematic name for the molecule below. (2 pts) Indicate whether the listed solvent is protic or aprotic. a. tert-butanol [(CH3)3COH] b. formamide (HCONH2]
1. (48 pts, 4 pts each) Give an acceptable IUPAC name for the following compound: CH) i 0 CO,H CH, OH Font Font COOH CH,_ch, bi-ch, bi-CH, CN CH OH CHO Font соон NO 2. (36 pts, 4 pts each) Draw a structure for the following compounds: a. 2-Amino-2-methylbutanol b. 4-Hexynol C. 3-Methoxycycloheptanecarboxylic acid d. 2-Phenylethanol e. 3-Hydroxycyclopentanecarboxamide f. 4-Bromobenzaldehyde Font g. 6-Bromohexanoic acid h. 2, 3, 4-Hexanetriol L1-Decanthi 3. (16 pts, 4 pts each) Draw a structural formula for...
4. Provide an acceptable name for the compounds (a-c) shown below. (6 points) CH3 "CHE a Br Name: b. CH3CH2CH2CH(CH3)CH2CHBr Name: Name:
12 5. Provide an acceptable mechanism for the formation of EACH of the four stereoisomers that are produced in the following reaction. Also provide the isomer relationship between each set of stereoisomers (64 pts). CH3 Нао" H3O+ 304 stereoisomers
12 5. Provide an acceptable mechanism for the formation of EACH of the four stereoisomers that are produced in the following reaction. Also provide the isomer relationship between each set of stereoisomers (64 pts). CH3 Нао" H3O+ 304 stereoisomers
14. (9 pts) Provide acceptable names for the structures drawn below. - NH2 Son Sant OCH3 HO
Provide the name for the following structures, or the structures
following names
a. (E)-Hept-2-en-5-yn
b. 3,4-dimethylpentanenitrile
12. (10 points) Provide the name for the following structures, or the structures for the following names: a. (E)-Hept-2-en-5-yn b. 3,4-Dimethylpentanenitrile CH3 CH3 H3c CH3 C. CH3 H3C H CH3 -CH3 d .