1. Write the products of the following reactions. If there is no reaction write NR. For full credit clearly indicate cis or trans relationships in cyclic compounds, where appropriate. a) + Cl2, w ater sol vent b) CH3 + Br,, water solvent c) -CH + Br,, water solvent D
1. Write the products of the following reactions. If there is no reaction write NR. For full credit clearly indicate cis or trans relationships in cyclic compounds, where appropriate. a) + Cl2, w ater sol vent b) CH3 + Br,, water solvent c) -CH + Br,, water solvent D
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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![**Instructions**: Write the products of the following reactions. If there is no reaction, write NR. For full credit, clearly indicate cis or trans relationships in cyclic compounds, where appropriate.
**a)** Hex-2-ene + Cl₂, water solvent → ?
**b)** Methylcyclohexene + Br₂, water solvent → ?
**c)** 1-Methyl-1-deuteriocyclohexene + Br₂, water solvent → ?
**d)** Hex-2-ene + KMnO₄, KOH, cold → ?
**e)** Methylcyclohexene + KMnO₄, KOH, cold → ?
**f)** 3-Methylpent-1-ene + H₂, 1 atm, RT, Ni (cat) → ?
**g)** 1-Phenylcyclohexene + H₂, 1 atm, RT, Ni (cat) → ?
**h)** 3-Methyl-1-butene:
1) H₂B∙THF
2) HOOH, NaOH, water solvent → ?
**i)** Cyclohexene:
1) H₂B∙THF
2) HOOH, NaOH, water solvent → ?
**j)** Methylcyclohexene:
1) H₂B∙THF
2) HOOH, NaOH, water solvent → ?
**k)** 3-Methylpent-1-ene:
1) Ozone
2) (CH₃)₂S → ?
**l)** 1-Methylcyclohexene:
1) Ozone
2) (CH₃)₂S → ?
**Notes**:
- Follow the mechanisms of each reaction to determine the correct structures.
- Consider stereochemistry for reactions involving cyclic compounds or chiral products.
- Use structural drawing for clarity where necessary.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F0b2d8d84-896e-4f9e-963b-da7844b9b0f5%2Fb7ab6469-858f-4af0-b5e7-325427731c44%2Fior45ci_processed.jpeg&w=3840&q=75)
Transcribed Image Text:**Instructions**: Write the products of the following reactions. If there is no reaction, write NR. For full credit, clearly indicate cis or trans relationships in cyclic compounds, where appropriate.
**a)** Hex-2-ene + Cl₂, water solvent → ?
**b)** Methylcyclohexene + Br₂, water solvent → ?
**c)** 1-Methyl-1-deuteriocyclohexene + Br₂, water solvent → ?
**d)** Hex-2-ene + KMnO₄, KOH, cold → ?
**e)** Methylcyclohexene + KMnO₄, KOH, cold → ?
**f)** 3-Methylpent-1-ene + H₂, 1 atm, RT, Ni (cat) → ?
**g)** 1-Phenylcyclohexene + H₂, 1 atm, RT, Ni (cat) → ?
**h)** 3-Methyl-1-butene:
1) H₂B∙THF
2) HOOH, NaOH, water solvent → ?
**i)** Cyclohexene:
1) H₂B∙THF
2) HOOH, NaOH, water solvent → ?
**j)** Methylcyclohexene:
1) H₂B∙THF
2) HOOH, NaOH, water solvent → ?
**k)** 3-Methylpent-1-ene:
1) Ozone
2) (CH₃)₂S → ?
**l)** 1-Methylcyclohexene:
1) Ozone
2) (CH₃)₂S → ?
**Notes**:
- Follow the mechanisms of each reaction to determine the correct structures.
- Consider stereochemistry for reactions involving cyclic compounds or chiral products.
- Use structural drawing for clarity where necessary.
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