Explain this whole mechanish ### Experiment 6: IR Spectroscopy#### Reaction Schemes and Descriptions**1. Conversion of Cyclohexanol to Cyclohexanone**- **Reactants:** Cyclohexanol- **Reagents:** NaOCl, AcOH, 45-50°C- **Product:** Cyclohexanone**Chemical Reaction:**\[ \text{Cyclohexanol} \xrightarrow{\text{NaOCl, AcOH, 45-50°C}} \text{Cyclohexanone} \]**2. Oxidation of Steroid Alcohol to Steroid Ketone**- **Reactants:** Steroid Alcohol- **Reagents:** MCPBA in CH₂Cl₂- **Product:** Steroid Ketone**Chemical Reaction:**\[ \text{Steroid Alcohol} \xrightarrow{\text{MCPBA, CH₂Cl₂}} \text{Steroid Ketone} \]**3. Formation of Phenyl Ether**- **Reactants:** Chlorobenzene and Phenol- **Reagents:** K₂CO₃- **Product:** Phenyl Ether**Chemical Reaction:**\[ \text{Chlorobenzene} + \text{Phenol} \xrightarrow{\text{K₂CO₃}} \text{Phenyl Ether} \]**4. Synthesis of Benzoic Acid via Grignard Reaction**- **Reactants:** Bromobenzene- **Reagents:** 1. Mg 2. CO₂- **Product:** Benzoic Acid**Chemical Reaction:**\[ \text{Bromobenzene} \xrightarrow{\text{1. Mg, 2. CO₂}} \text{Benzoic Acid} \]**5. Reduction of Benzylideneacetophenone to 1,2-Diphenylethane-1,2-diol**- **Reactants:** Benzylideneacetophenone- **Reagents:** NaBH₄, EtOH- **Product:** 1,2-Diphenylethane-1,2-diol**Chemical Reaction:**\[ \text{Benzylideneacetophenone} \xrightarrow{\text{NaBH₄, EtOH}} \text{1,2-Diphenylethane-1,

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Answered: Explain this whole mechanish

Science

Chemistry

Explain this whole mechanish

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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Question

Explain this whole mechanish

### Experiment 6: IR Spectroscopy

#### Reaction Schemes and Descriptions

**1. Conversion of Cyclohexanol to Cyclohexanone**
- **Reactants:** Cyclohexanol
- **Reagents:** NaOCl, AcOH, 45-50°C
- **Product:** Cyclohexanone

**Chemical Reaction:**
\[ \text{Cyclohexanol} \xrightarrow{\text{NaOCl, AcOH, 45-50°C}} \text{Cyclohexanone} \]

**2. Oxidation of Steroid Alcohol to Steroid Ketone**
- **Reactants:** Steroid Alcohol
- **Reagents:** MCPBA in CH₂Cl₂
- **Product:** Steroid Ketone

**Chemical Reaction:**
\[ \text{Steroid Alcohol} \xrightarrow{\text{MCPBA, CH₂Cl₂}} \text{Steroid Ketone} \]

**3. Formation of Phenyl Ether**
- **Reactants:** Chlorobenzene and Phenol
- **Reagents:** K₂CO₃
- **Product:** Phenyl Ether

**Chemical Reaction:**
\[ \text{Chlorobenzene} + \text{Phenol} \xrightarrow{\text{K₂CO₃}} \text{Phenyl Ether} \]

**4. Synthesis of Benzoic Acid via Grignard Reaction**
- **Reactants:** Bromobenzene
- **Reagents:**
1. Mg
2. CO₂
- **Product:** Benzoic Acid

**Chemical Reaction:**
\[ \text{Bromobenzene} \xrightarrow{\text{1. Mg, 2. CO₂}} \text{Benzoic Acid} \]

**5. Reduction of Benzylideneacetophenone to 1,2-Diphenylethane-1,2-diol**
- **Reactants:** Benzylideneacetophenone
- **Reagents:** NaBH₄, EtOH
- **Product:** 1,2-Diphenylethane-1,2-diol

**Chemical Reaction:**
\[ \text{Benzylideneacetophenone} \xrightarrow{\text{NaBH₄, EtOH}} \text{1,2-Diphenylethane-1,

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