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Draw and label the E and Z isomers of each of the following compounds:
a. 2-pentene
b. 3-chloro-4-ethyl-2-methyloct-3-ene
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- Draw the structures of each of the following compounds:a. cis-1,3-Dibromocyclopentaneb. trans-1,2-Dimethylcyclobutanec. cis-1,2-Dichlorocyclopropaned. trans-1,4-DiethylcyclohexaneUsing bond lines draw the structures of the following compounds: a. 5-ethyl-2-methyl-3-heptyne b. Cyclopentylcyclohexane c. 1-isopropyl-4-ethylcyclohexene d. 3-isobutyl-5-propylnonane e. 4-ethyl-3-methyl-2-heptene f. 6-methyl-5-phenyl-2-octyneDraw the structure of each of the following compounds:a. Propanoneb. 2-Pentanonec. 3-Heptanoned. 2,4-Dimethyl-3-pentanone
- Draw all possible stereoisomers for each of the following: a. 2-chloro-3-hexanol b. 2-bromo-4-chlorohexane c. 2,3-dichloropentane d. 1,3-dibromopentaneDraw a condensed structure for each of the following: a. 2-hexyne b. 5-ethyl-3-octyne c. methylacetylene d. vinylacetylene e. methoxyethyne g. 1-bromo-1-pentyne h. 5-methyl-2-cyclohexeno i. diethylacetylene j. di-tert-butylacetylene k. cyclopentylacetylene l l. 5,6-dimethyl-2-heptyneDraw a condensed structure for each of the following: a. 2-hexyne b. 5-ethyl-3-octyne c. methylacetylene d. vinylacetylene e. methoxyethyne f. sec-butyl-tert-butylacetylene g. 1-bromo-1-pentyne h. 5-methyl-2-cyclohexenol i. diethylacetylene j. di-tert-butylacetylene k. cyclopentylacetylene l. 5,6-dimethyl-2-heptyne
- Name the following compound according to IUPAC nomenclature: a. 2,2-Dimethyl-5-fluoro-hept-3yne b. 3-Flouro-4-yne-heptane c. 3-Fluoro-6,6-dimethyl-hept-4-yne d. 4-Fluoro-2,2-dimethyl-3-heptynes: On A.What is the condensed structural formula of: 1. Methanol 2. Benzoic Acid 3. Methyl Benzoate 4. 1- Pentanol 5. Acetic Acid 6. Pentyl acetate 7. 1-octanol 8. Octyl acetate 9. Benzylic alcohol 10. Benzyl acetate 11. 1-Propanol 12. Propyl acetate Accessibility: Good to go hp1. An alkene reacts with water with an acid catalyst results into a formation of: A. Aldehyde B. Ketone C. Alcohol D. Ester 2. 3-Methylhexanal with K2Cr2O7 will yield: A. 3-Methyl-1-hexanol B. 3-Methylhexanoic acid C. 3-Methyl-1-hexanone D. 3-Methyl-1-hexanethiol 3. This is a reverse process of Hydration reaction: A. Oxidation reaction B. Reduction reaction C. Dehydration reaction D. Hydration reaction 4. Acetic acid reacts with a strong base forms: A. Salt B. Water C. Salt and Water D. No reaction 5. Ketones can be further oxidized with benedict's solution into: A. Alcohol B. Aldehyde C. Catalysts D. No reaction
- 3. For the following questions, refer to the structures in the table: A. B. a CH3 H₂C H₂C- CH3 CH₂CH₂CH3 C. trans-1-ethyl-3- isopropylcyclohexane D. H3C CH3 3.1 What is the IUPAC name of the compound in A. 3.2 What is the IUPAC name of the compound in B. 3.3 Draw the other five Newman projections of the molecule in B (using the drawn structure as the first Newman Projection). Label your drawings with numeral numbers (II-VI). Determine which among the drawn structures is the most stable Newman projection and justify your answer. 3.4 Draw the chair and flipped chair conformation of the molecule in C. Show with an equilibrium arrow which is more stable and justify your answer. 3.5 Write is the balanced equation (use chemical formulas) when the molecule in compound D undergoes a complete combustion?What is the IUPAC name for the following compound? CH₂CH₂ C CH3-CH₂-CH-CH₂-CH-CH-CH-CH₂ CI CH3 Select one: O A. 3,7-dichloro-5-ethyl-6-methyloctane O B. 2-chloro-3-methyl-4-(2-chlorobutyl) hexane O C. 2,6-dichloro-4-ethyl-3-methyloctane O D. 3-chloro-5-(2-chloro-1-methylpropyl) heptane OE. 2,3,4,6-dichloroethylmethyoctaneCH₂ CH₂CH3 The correct name for the compound given above is Select one: O a. 1-propyl-3-ethyl-4-methylbenzene b. 4-cyclopropyl-2-ethyl-1-methylbenzene O c. p,o-methylethylcyclopropylbenzene O d. 1-propyl-3-ethyl-4-methylcyclohexane