The major product obtained in the given reaction has to be identified. Concept Introduction: Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond ( alkene ). Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides. Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

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Answer 1

Question

Chapter 8.4, Problem 5CC

(a)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

(b)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

(c)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

(d)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

(e)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

(f)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

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Students have asked these similar questions

There is an instrument in Johnson 334 that measures total-reflectance x-ray fluorescence (TXRF) to do elemental analysis (i.e., determine what elements are present in a sample). A researcher is preparing a to measure calcium content in a series of well water samples by TXRF with an internal standard of vanadium (atomic symbol: V). She has prepared a series of standard solutions to ensure a linear instrument response over the expected Ca concentration range of 40-80 ppm. The concentrations of Ca and V (ppm) and the instrument response (peak area, arbitrary units) are shown below. Also included is a sample spectrum. Equation 1 describes the response factor, K, relating the analyte signal (SA) and the standard signal (SIS) to their respective concentrations (CA and CIS). Ca, ppm V, ppm SCa, arb. units SV, arb. units 20.0 10.0 14375.11 14261.02 40.0 10.0 36182.15 17997.10 60.0 10.0 39275.74 12988.01 80.0 10.0 57530.75 14268.54 100.0…

A mixture of 0.568 M H₂O, 0.438 M Cl₂O, and 0.710 M HClO are enclosed in a vessel at 25 °C. H₂O(g) + C₁₂O(g) = 2 HOCl(g) K = 0.0900 at 25°C с Calculate the equilibrium concentrations of each gas at 25 °C. [H₂O]= [C₁₂O]= [HOCI]= M Σ M

What units (if any) does the response factor (K) have? Does the response factor (K) depend upon how the concentration is expressed (e.g. molarity, ppm, ppb, etc.)?

Answer 2

Question

Chapter 8.4, Problem 5CC

(a)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

(b)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

(c)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

(d)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

(e)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

(f)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

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Answer 3

Question

Chapter 8.4, Problem 5CC

(a)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

(b)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

(c)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

(d)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

(e)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

(f)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

Expert Solution & Answer

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Answer 4

Question

Chapter 8.4, Problem 5CC

(a)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

(b)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

(c)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

(d)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

(e)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

(f)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

Expert Solution & Answer

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Answer 5

Chapter 8.4, Problem 5CC

(a)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

(b)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

(c)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

(d)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

(e)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

(f)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

Answer 6

Chapter 8.4, Problem 5CC

(a)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

Answer 7

Chapter 8.4, Problem 5CC

(a)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

Answer 8

(b)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

Answer 9

(b)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

Answer 10

(c)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

Answer 11

(c)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

Answer 12

(d)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

Answer 13

(d)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

Answer 14

(e)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

Answer 15

(e)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

Answer 16

(f)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

Answer 17

(f)

Interpretation Introduction

Interpretation:

The major product obtained in the given reaction has to be identified.

Concept Introduction:

Hydro-halogenation reaction: In this reaction, hydrogen halide added across the unsaturated bond (alkene).

Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.

Anti-Markovnikov’s rule: An unsymmetrical alkene reacts with hydrogen halide in which halide ions goes to the less substitution position of carbon-carbon double bond which provides alkyl halides.

Answer 18

Expert Solution & Answer

Answer 19

Expert Solution & Answer

Answer 20

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Answer 21

Ch. 8.4 - Prob. 1CC Ch. 8.4 - Prob. 2CC Ch. 8.4 - Draw a mechanism for the following...Ch. 8.4 - Prob. 3PTS Ch. 8.4 - Prob. 4ATS Ch. 8.4 - Prob. 5CC Ch. 8.4 - Prob. 2LTS Ch. 8.4 - Prob. 6PTS Ch. 8.5 - Prob. 8CC Ch. 8.5 - Prob. 9CC

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