Provide the name for the following structures, or the structures following names
a. (E)-Hept-2-en-5-yn
b. 3,4-dimethylpentanenitrile
Provide the name for the following structures, or the structures following names a. (E)-Hept-2-en-5-yn b. 3,4-dimethylpentanenitrile...
Problem 5. Provide IUPAC names for the following organic structures, and include (R)/(S) in the naming if needed. (8p) Br a) b) Br F F c) CH3 d) H3C
6. Provide IUPAC names for the following compounds (E-G). Name: H₃ C. CH3 CH, E Name: H₃C CH3 CH F Name: HO OH сна G
2. Provide IUPAC names for the following compounds (E-G). Name: НАС. eo CH3 CH3 E i Name: Н4С CH3 'N H CH3 F o Name: HO OH CH3 G
Draw structures corresponding to the following names: 9.19 Draw structures corresponding to the following names: (b) 3-Ethyl-5-methyl-1,6,8-decatriyne (a) 3,3-Dimethyl-4-octyne (c) 2,2,5,5-Tetramethyl-3-hexyne (d) 3,4-Dimethylcyclodecyne (e) 3,5-Heptadien-1-yne (g) 3-sec-Butyl-1-heptyne (f) 3-Chloro-4,4-dimethyl-1-nonen-6-yne (h) S-tert-Butyl-2-methyl-3-octyne 9.19 Draw structures corresponding to the following names: (b) 3-Ethyl-5-methyl-1,6,8-decatriyne (a) 3,3-Dimethyl-4-octyne (c) 2,2,5,5-Tetramethyl-3-hexyne (d) 3,4-Dimethylcyclodecyne (e) 3,5-Heptadien-1-yne (g) 3-sec-Butyl-1-heptyne (f) 3-Chloro-4,4-dimethyl-1-nonen-6-yne (h) S-tert-Butyl-2-methyl-3-octyne
Give the IUPAC name for the following structures: Part II: Give the IUPAC name for each of the following structures. (10 marks) 1. нс. CH CH3 CH3 2. нс. CH3 CH3 CH3 3 -CH3 CH3 CH3 4. F CH3 CI 5. À 6. HC CH3 Br CH3 H 7. H 8. H3C 9. HC CI HC CHE 10. H3c CH3
Provide the name the following four alkenes and use E/Z prefixes to specify the geometry for each. H3C H CH3 = c H3C-HC CH₂ - CH₂ - CH₂ CH3 Hac
Name the structures using IUPAC names 2. Name the structures using IUPAC names: Br е. а. C. Br b. d. Include the RS designation in the name. - а. C. b. d. f. а. b. d. CI
- 6! Name the following compounds based on their structures (circle your answer) (6 pts tot сн. CH,CH.CH) a) eis-5-methylhex-2-ene b) trans-5-methylhex-2-ene eis-2-methylhex-3-ene d) trans-2-methylhex-3-ene 2) A - H _ CH CHCH a) 3-methylbut-3-ene 62-ethylprop-1-ene c)2-methylbut-1-ene d) 2-ethylprop-2-ene hepta-2,6-diene b) hept-2,6-diene c) hepta-1,5-diene d) hept-1,5-diene сн. (H,сне H a) (E)-3-methylhex-3-ene b) (Z)-3-methylhex-3-ene (E)-4-methylhex-3-ene a) (2)-4-methylhex-3-ene CHÚCH). a 3-methylcyclopentene $) methylcyclopentene c) 5-methylcyclopentene CH3 a) 2,5-dimethylcyclohexa-1,5-diene 1,4-dimethylcyclohexa-1,3-diene c) 1,4-dimethylcyclohexa-4,6-diene Hoa
4. Draw structures for the following compounds (12 points): a. 6,6-dimethylhept-2-yne b. 5-amino-4-methoxyhept-6-yn-2-ol c. 4-bromo-4-methyl-2-cyclohexenol d. (S)-2-chlorohexane e. (2S,3S)-2,3-butanediol f. (R)-3-bromocyclopentene
1. Draw the structures of: a) (Z) 2-iodo-3-methyl-2-heptene b) cis non-3-en-5 yne Give the IUPAC name of the following compounds, including steochemistry. a) F CH2CH2Br CH3CE 2. a) Draw the most stable chair conformation of cis 1,3-difluorocyclohexane. b) Draw a Newman projection of 2-iodo-3-methylpentane looking down the 3. Compound X has the formula CoHB2Br4. Compound X reacts with excess H2/Pd to give CATHa6Bra. How many does compound X have? Show how you got your answer. rings 4. For each pair...