What is the major product of these reactions? Could you explain how you got the products? ### Image Transcription for Educational Website#### Chemical Reactions**d)** A chemical reaction involving:- A ketone compound: - ![attach molecule image] with a formula containing a ketone group.- Mixed with a diethyl phosphorochloridate compound: - ![attach molecule image] a triphosphate ester.- This reaction proceeds using: - **NaOH/H₂O & heptane** as the medium. - **Aliquat 336** as the phase-transfer catalyst.---**e)** A multi-step reaction involving:1. Starting with an alkyl halide: - ![attach molecule image] with a chlorine atom.2. Reacted with **Mg in ether** to form a Grignard reagent.3. Sequential reaction: - **H** indicates acid-workup with an aromatic ketone. - [second structure] **H⁺/H₂O** for aqueous acidic workup.---**f)** A two-step reaction involving:1. Starting with an amide compound: - ![attach molecule image] with a methyl and an aromatic group.2. Reactions proceed with: - **H₂O, H₂SO₄, Δ** indicating hydrolysis under acidic and heat conditions.3. Finally treated with: - **NH₄OH** for neutralization or a modification step.---These chemical processes illustrate important methods in organic synthesis, including Grignard reaction formation and hydrolysis under acidic conditions, useful in constructing complex organic molecules.

d. This is a type of Witting reaction. It leads to the formation of trans-alkene. e. This is a…

Answered: d) NaOH/H;O & heptane OEt OEt Aliquat…

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Chemistry

d) NaOH/H;O & heptane OEt OEt Aliquat 336 1) Mg in ether e) H. 2) 3) H*/H2O f) 1) H20, H2SO4, A NH 2) NH,OH

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter18: Functional Derivatives Of Carboxylic Acids

Section: Chapter Questions

Problem 18.69P

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Concept explainers

Types of Polymers on the basis of Method of Preparation

Question

What is the major product of these reactions? Could you explain how you got the products?

### Image Transcription for Educational Website

#### Chemical Reactions

**d)** A chemical reaction involving:
- A ketone compound:
- ![attach molecule image] with a formula containing a ketone group.
- Mixed with a diethyl phosphorochloridate compound:
- ![attach molecule image] a triphosphate ester.
- This reaction proceeds using:
- **NaOH/H₂O & heptane** as the medium.
- **Aliquat 336** as the phase-transfer catalyst.

---

**e)** A multi-step reaction involving:
1. Starting with an alkyl halide:
- ![attach molecule image] with a chlorine atom.
2. Reacted with **Mg in ether** to form a Grignard reagent.
3. Sequential reaction:
- **H** indicates acid-workup with an aromatic ketone.
- [second structure] **H⁺/H₂O** for aqueous acidic workup.

---

**f)** A two-step reaction involving:
1. Starting with an amide compound:
- ![attach molecule image] with a methyl and an aromatic group.
2. Reactions proceed with:
- **H₂O, H₂SO₄, Δ** indicating hydrolysis under acidic and heat conditions.
3. Finally treated with:
- **NH₄OH** for neutralization or a modification step.

---

These chemical processes illustrate important methods in organic synthesis, including Grignard reaction formation and hydrolysis under acidic conditions, useful in constructing complex organic molecules.

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