IUPAC NOMENCLATURE of organic compounds.
3. (8 pts) Assign unambiguous syste structures. unambiguous systematic names to each of the following parent:...
1. (9 pts) Assign a systematic name for each of the following compounds:
Give IUPAC names for the following compounds: Draw structures corresponding to each of the given names. A. 2-phenyl-2-propanol B. 2, 3-diphenyl-2-hexene C. 2-hydroxyacetophenone D. 5, 5-dimcthyl-l, 3, 6-cycloheptatriene-l-carboxylicacid E. Acetic anhydride
(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]
Provide IUPAC names for each of the following structures: Draw structures corresponding to each of the following names: 6. 2-propenamide 7. 3,4,5-trimethoxybenzoyl chloride 8. acetic formic anhydride 9. N,N-dimethylformamide 10. methyl cis-3-ethylcyclobutanecarboxylate 11. (E)-2,4-dimethyl-2-hexenoyl chloride
please help 3. Please draw the structures for the major product(s) from each of the following reactions and include stereochemistry where appropriate. (2 pts for each) (a) O2N NH2 NO2 (b) NAOCH3 OCH3 CHон (c) pyridine -NH2 + S-Cl (d) HOH CHO Br2 HO H Нао H OH H-OH CH2OH (e) Hао* Ph H (f) N2HA H (hint: cyclization) 3. Please draw the structures for the major product(s) from each of the following reactions and include stereochemistry where appropriate. (2...
3. Give good systematic names of the following. Include E,Z nomenclature if necessary. Parts A-C 4. Identify the following as nucleophiles (Nu) or electrophiles (E). Figures 1-5 bve good systematic names for the following. Include E,Z nomenclature if necessary. a. b. C. Cl 4. Identify the following as nucleophiles (Nu) or electrophiles (E) Ho (CHa) C H20 BF3
1. Name the following or Draw the Structure (2 x 3 pts each) a. N-methyl-3-phenylpentan-2-amine OH b. OH NH2O 2. Draw the starting materials for the following hydrolysis reactions. (3 pts each) 1. NaOH, H2O a. 3-or 2. HCI, H2O OH OH Ph 1. NaOH, H2O b. HO Н. CH3 OH HPh 2. HCI, H2O 3. Of the following, which form would actually exist at: (5 points) a) pH = 2 (acidic) b) pH = 7 (neutral) c) pH =...
1. Give systematic IUPAC names for each of the following: CH3CH2C(CH3)2CH(CH2CH3)CH3 CH3C(CH3)CH2 CH2O CH3CH(NH2)CH3 CH3OCH2CH2CH3 CH(CH3)2COOH For the list above I currently put the following as the IUPAC names. If any are wrong can you please correct them! Give systematic IUPAC names for each of the following: CH3CH2C(CH3)2CH(CH2CH3)CH3 IUPAC Name: 3,3,4-trimethylhexane IUPAC Name: 3-methyl-4-ol-heptane CH3C(CH3)CH2 IUPAC Name: 2-methylpropene CH2O IUPAC Name: methanal CH3CH(NH2)CH3 IUPAC Name: isopropylamine CH3OCH2CH2CH3 IUPAC Name: methoxyethane (ethyl methyl ether) CH(CH3)2COOH IUPAC Name: 2-methylpropanoic acid
write condensed structures fore each of the following compounds Homework Problems 7.1 Write condensed structures for each of the following compounds: a. 2,2,4-trimethylpentane b. 5-isopropyl-2-methyloctane c. 1,1,3,3-tetrabromopropane d. 1,1-dichlorocyclopentane e. 1,4-diethylcyclohexane f. 1-bromo-2-methylcyclobutane What are the IUPAC names of the following compounds? 7.2 CH2CH, CH3 a) CH, C CH, CH, CH СH,CH, сн, CH2CH, b) CH2CH d) (CH),CCH2CH e) F Br Br Write the structural formulas and names for FOUR isomers of cycloalkane, CSH10. 7.3 7.4 Propose structures for molecules...
4) The following compounds are incorrectly named. Provide correct systematic names for each a. 2-methyl-2-ethylpropane b. 2,6-diethylcyclohexane c. 1-bromo-3-isopropylpentane d. 5-fluoro-8-methyl-3-tert-butylnonane