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

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Chapter1: Chemical Foundations
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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.
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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