(1) Write a complete chemical equation showing reactants, products, and catalys needed (if any) for the following reaction and (2) Draw and name the organi compound found in every reaction. (a) Complete hydrogenation of 2-Methylhexa-1,5-diene (b) Complete halogenation (Br2) of 3-Ethyl-2,2-dimethylhept-3-ene (c) Reaction of (4E)-2,4-Dimethylhexa-1,4-diene with a mole of water (d) Reaction of cis-3,3-Dimethyl-4-propylocta-1,5-diene with two mole of HBr (e) Reaction of trans-1-Bromo-3-chlorocyclopentane with potassium hydroxide (f) Formation of Gilman reagent using isopropyl bromide (g) Ozonolysis of 3,3-Dimethyloct-4-yne (h) Complete halogenation (Cl2) of 3-Ethyl-5-methyl-1,6,8-decatriyne (i) Partial hydrogenation using Lindlar's Catalyst 2,2,5,5-Tetramethylhex-3-yne (i) Reaction of 3,4-Dimethylcyclodecyne with sodium amide

Chemistry: The Molecular Science
5th Edition
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:John W. Moore, Conrad L. Stanitski
Chapter6: Covalent Bonding
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Problem 24QRT
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(1) Write a complete chemical equation showing reactants, products, and catalysts
needed (if any) for the following reaction and (2) Draw and name the organic
compound found in every reaction.
(a) Complete hydrogenation of 2-Methylhexa-1,5-diene
(b) Complete halogenation (Br2) of 3-Ethyl-2,2-dimethylhept-3-ene
(c) Reaction of (4E)-2.4-Dimethylhexa-1,4-diene with a mole of water
(d) Reaction of cis-3,3-Dimethyl-4-propylocta-1,5-diene with two mole of HBr
(e) Reaction of trans-1-Bromo-3-chlorocyclopentane with potassium hydroxide
(f) Formation of Gilman reagent using isopropyl bromide
(g) Ozonolysis of 3,3-Dimethyloct-4-yne
(h) Complete halogenation (Cl2) of 3-Ethyl-5-methyl-1,6,8-decatriyne
(i) Partial hydrogenation using Lindlar's Catalyst 2,2,5,5-Tetramethylhex-3-yne
(i) Reaction of 3.4-Dimethylcyclodecyne with sodium amide
Transcribed Image Text:(1) Write a complete chemical equation showing reactants, products, and catalysts needed (if any) for the following reaction and (2) Draw and name the organic compound found in every reaction. (a) Complete hydrogenation of 2-Methylhexa-1,5-diene (b) Complete halogenation (Br2) of 3-Ethyl-2,2-dimethylhept-3-ene (c) Reaction of (4E)-2.4-Dimethylhexa-1,4-diene with a mole of water (d) Reaction of cis-3,3-Dimethyl-4-propylocta-1,5-diene with two mole of HBr (e) Reaction of trans-1-Bromo-3-chlorocyclopentane with potassium hydroxide (f) Formation of Gilman reagent using isopropyl bromide (g) Ozonolysis of 3,3-Dimethyloct-4-yne (h) Complete halogenation (Cl2) of 3-Ethyl-5-methyl-1,6,8-decatriyne (i) Partial hydrogenation using Lindlar's Catalyst 2,2,5,5-Tetramethylhex-3-yne (i) Reaction of 3.4-Dimethylcyclodecyne with sodium amide
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