The intermediate in first step of given halogenation reaction has to be drawn. Concept Introduction: Halogenation of Alkynes : Intermediate: It is a molecular entity formed from the reactants and then reacts further to give the products. Alkynes react with excess of halogens in presence of carbon tetrachloride to form tetrahalo-substituted compound.

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Answer 1

Question

Chapter 9, Problem 70IP

(a)

Interpretation Introduction

Interpretation:

The intermediate in first step of given halogenation reaction has to be drawn.

Concept Introduction:

Halogenation of Alkynes:

Intermediate: It is a molecular entity formed from the reactants and then reacts further to give the products.

Alkynes react with excess of halogens in presence of carbon tetrachloride to form tetrahalo-substituted compound.

(b)

Interpretation Introduction

Interpretation:

During the second step of halogenation mechanism, a high energy carbocation is formed which has to be drawn and explained.

Concept Introduction:

Halogenation of Alkynes:

Alkynes react with excess of halogens in presence of carbon tetrachloride to form tetrahalo-substituted compound.

(c)

Interpretation Introduction

Interpretation:

The reaction mechanism of halogenation with both steps has to be given.

Concept Introduction:

Halogenation of Alkynes:

Alkynes react with excess of halogens in presence of carbon tetrachloride to form tetrahalo-substituted compound.

Mechanism of the reaction is the step-by-step description of the process by which reactants are changed into products.

Curved arrows show the bonds that are formed and the bonds that are broken in a reaction.

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Please help, this is all the calculations i got!!! I will rate!!!Approx mass of KMnO in vial: 3.464 4 Moss of beaker 3×~0. z Nax200: = 29.9219 Massof weacerv after remosimgain N2C2O4. Need to fill in all the missing blanks. ง ง Approx mass of KMnO4 in vials 3.464 Mass of beaker + 3x ~0-304: 29.9219 2~0.20 Miss of beaker + 2x- 29.7239 Mass of beaker + 1x~0.2g Naz (204 29-5249 Mass of beaver after removing as qa Na₂ C₂O T1 T2 T3 Final Buiet reading Initial butet reading (int)) Hass of NaOr used for Titration -reading (mL) calculation Results: 8.5ml 17mL 27.4mL Oml Om Oml T1 T2 T3 Moles of No CO Moles of KMO used LOF KM. O used Molenty of KMNO Averagem Of KMOWL

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Answer 2

Question

Chapter 9, Problem 70IP

(a)

Interpretation Introduction

Interpretation:

The intermediate in first step of given halogenation reaction has to be drawn.

Concept Introduction:

Halogenation of Alkynes:

Intermediate: It is a molecular entity formed from the reactants and then reacts further to give the products.

Alkynes react with excess of halogens in presence of carbon tetrachloride to form tetrahalo-substituted compound.

(b)

Interpretation Introduction

Interpretation:

During the second step of halogenation mechanism, a high energy carbocation is formed which has to be drawn and explained.

Concept Introduction:

Halogenation of Alkynes:

Alkynes react with excess of halogens in presence of carbon tetrachloride to form tetrahalo-substituted compound.

(c)

Interpretation Introduction

Interpretation:

The reaction mechanism of halogenation with both steps has to be given.

Concept Introduction:

Halogenation of Alkynes:

Alkynes react with excess of halogens in presence of carbon tetrachloride to form tetrahalo-substituted compound.

Mechanism of the reaction is the step-by-step description of the process by which reactants are changed into products.

Curved arrows show the bonds that are formed and the bonds that are broken in a reaction.

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Answer 3

Question

Chapter 9, Problem 70IP

(a)

Interpretation Introduction

Interpretation:

The intermediate in first step of given halogenation reaction has to be drawn.

Concept Introduction:

Halogenation of Alkynes:

Intermediate: It is a molecular entity formed from the reactants and then reacts further to give the products.

Alkynes react with excess of halogens in presence of carbon tetrachloride to form tetrahalo-substituted compound.

(b)

Interpretation Introduction

Interpretation:

During the second step of halogenation mechanism, a high energy carbocation is formed which has to be drawn and explained.

Concept Introduction:

Halogenation of Alkynes:

Alkynes react with excess of halogens in presence of carbon tetrachloride to form tetrahalo-substituted compound.

(c)

Interpretation Introduction

Interpretation:

The reaction mechanism of halogenation with both steps has to be given.

Concept Introduction:

Halogenation of Alkynes:

Alkynes react with excess of halogens in presence of carbon tetrachloride to form tetrahalo-substituted compound.

Mechanism of the reaction is the step-by-step description of the process by which reactants are changed into products.

Curved arrows show the bonds that are formed and the bonds that are broken in a reaction.

Expert Solution & Answer

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Answer 4

Question

Chapter 9, Problem 70IP

(a)

Interpretation Introduction

Interpretation:

The intermediate in first step of given halogenation reaction has to be drawn.

Concept Introduction:

Halogenation of Alkynes:

Intermediate: It is a molecular entity formed from the reactants and then reacts further to give the products.

Alkynes react with excess of halogens in presence of carbon tetrachloride to form tetrahalo-substituted compound.

(b)

Interpretation Introduction

Interpretation:

During the second step of halogenation mechanism, a high energy carbocation is formed which has to be drawn and explained.

Concept Introduction:

Halogenation of Alkynes:

Alkynes react with excess of halogens in presence of carbon tetrachloride to form tetrahalo-substituted compound.

(c)

Interpretation Introduction

Interpretation:

The reaction mechanism of halogenation with both steps has to be given.

Concept Introduction:

Halogenation of Alkynes:

Alkynes react with excess of halogens in presence of carbon tetrachloride to form tetrahalo-substituted compound.

Mechanism of the reaction is the step-by-step description of the process by which reactants are changed into products.

Curved arrows show the bonds that are formed and the bonds that are broken in a reaction.

Expert Solution & Answer

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Answer 5

Chapter 9, Problem 70IP

(a)

Interpretation Introduction

Interpretation:

The intermediate in first step of given halogenation reaction has to be drawn.

Concept Introduction:

Halogenation of Alkynes:

Intermediate: It is a molecular entity formed from the reactants and then reacts further to give the products.

Alkynes react with excess of halogens in presence of carbon tetrachloride to form tetrahalo-substituted compound.

(b)

Interpretation Introduction

Interpretation:

During the second step of halogenation mechanism, a high energy carbocation is formed which has to be drawn and explained.

Concept Introduction:

Halogenation of Alkynes:

Alkynes react with excess of halogens in presence of carbon tetrachloride to form tetrahalo-substituted compound.

(c)

Interpretation Introduction

Interpretation:

The reaction mechanism of halogenation with both steps has to be given.

Concept Introduction:

Halogenation of Alkynes:

Alkynes react with excess of halogens in presence of carbon tetrachloride to form tetrahalo-substituted compound.

Mechanism of the reaction is the step-by-step description of the process by which reactants are changed into products.

Curved arrows show the bonds that are formed and the bonds that are broken in a reaction.

Answer 6

Chapter 9, Problem 70IP

(a)

Interpretation Introduction

Interpretation:

The intermediate in first step of given halogenation reaction has to be drawn.

Concept Introduction:

Halogenation of Alkynes:

Intermediate: It is a molecular entity formed from the reactants and then reacts further to give the products.

Alkynes react with excess of halogens in presence of carbon tetrachloride to form tetrahalo-substituted compound.

Answer 7

Chapter 9, Problem 70IP

(a)

Interpretation Introduction

Interpretation:

The intermediate in first step of given halogenation reaction has to be drawn.

Concept Introduction:

Halogenation of Alkynes:

Intermediate: It is a molecular entity formed from the reactants and then reacts further to give the products.

Alkynes react with excess of halogens in presence of carbon tetrachloride to form tetrahalo-substituted compound.

Answer 8

(b)

Interpretation Introduction

Interpretation:

During the second step of halogenation mechanism, a high energy carbocation is formed which has to be drawn and explained.

Concept Introduction:

Halogenation of Alkynes:

Alkynes react with excess of halogens in presence of carbon tetrachloride to form tetrahalo-substituted compound.

Answer 9

(b)

Interpretation Introduction

Interpretation:

During the second step of halogenation mechanism, a high energy carbocation is formed which has to be drawn and explained.

Concept Introduction:

Halogenation of Alkynes:

Alkynes react with excess of halogens in presence of carbon tetrachloride to form tetrahalo-substituted compound.

Answer 10

(c)

Interpretation Introduction

Interpretation:

The reaction mechanism of halogenation with both steps has to be given.

Concept Introduction:

Halogenation of Alkynes:

Alkynes react with excess of halogens in presence of carbon tetrachloride to form tetrahalo-substituted compound.

Mechanism of the reaction is the step-by-step description of the process by which reactants are changed into products.

Curved arrows show the bonds that are formed and the bonds that are broken in a reaction.

Answer 11

(c)

Interpretation Introduction

Interpretation:

The reaction mechanism of halogenation with both steps has to be given.

Concept Introduction:

Halogenation of Alkynes:

Alkynes react with excess of halogens in presence of carbon tetrachloride to form tetrahalo-substituted compound.

Mechanism of the reaction is the step-by-step description of the process by which reactants are changed into products.

Curved arrows show the bonds that are formed and the bonds that are broken in a reaction.

Answer 12

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Answer 13

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Answer 14

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Answer 15

Ch. 9.2 - Prob. 1LTS Ch. 9.2 - Prob. 1PTS Ch. 9.2 - Prob. 2PTS Ch. 9.2 - Prob. 3PTS Ch. 9.2 - (+)-Citronella is the main compound responsible...Ch. 9.3 - Prob. 2LTS Ch. 9.3 - Prob. 5PTS Ch. 9.3 - Prob. 6ATS Ch. 9.4 - Prob. 7CC Ch. 9.4 - Prob. 8CC

Interpretation: During the second step of halogenation mechanism, a high energy carbocation is formed which has to be drawn and explained. Concept Introduction: Halogenation of Alkynes: Alkynes react with excess of halogens in presence of carbon tetrachloride to form tetrahalo-substituted compound.

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