Organic Chemistry (9th Edition)
Organic Chemistry (9th Edition)
9th Edition
ISBN: 9780321971371
Author: Leroy G. Wade, Jan W. Simek
Publisher: PEARSON
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Chapter 6.8, Problem 6.13P

(a)

Interpretation Introduction

Interpretation:

The rate of the reaction between 0.5M 1bromobutane and the changed concentration of sodium methoxide, that is 2.0M instead of 1.0M NaHCO3, is to be predicted.

Concept introduction:

The replacement or substitution of one functional group with another different functional group in any chemical reaction is termed as substitution reaction.

The nucleophilic reaction that contains a substrate as well as a nucleophile as the reactants which means a bimolecular nucleophilic reaction is termed as SN2 reaction. It includes the bond-making and bond-breaking steps. This is a one-step reaction in which both nucleophile and substrate participate in the rate determining step.

(b)

Interpretation Introduction

Interpretation:

The reactants, the transition state, and the products for the reaction between 1bromobutane and excess of ammonia are to be drawn.

Concept introduction:

The replacement or substitution of one functional group with another different functional group in any chemical reaction is termed as substitution reaction.

The nucleophilic reaction that contains only a substrate as a reactant and not a nucleophile, which means a unimolecular nucleophilic reaction, is termed as SN1 reaction.

The nucleophilic reaction that contains a substrate as well as a nucleophile as the reactants, which means a bimolecular nucleophilic reaction, is termed as SN2 reaction. It includes the bond-making and bond-breaking steps. This is a one-step reaction in which both nucleophile and substrate participate in the rate determining step.

(c)

Interpretation Introduction

Interpretation:

The different SN2 reaction that involves different combination of an alkoxide and an alkyl bromide that produces 1methoxybutane is to be shown.

Concept introduction:

The replacement or substitution of one functional group with another different functional group in any chemical reaction is termed as substitution reaction.

The nucleophilic reaction that contains only a substrate as a reactant and not a nucleophile, which means a unimolecular nucleophilic reaction, is termed as SN1 reaction.

The nucleophilic reaction that contains a substrate as well as a nucleophile as the reactants, which means a bimolecular nucleophilic reaction, is termed as SN2 reaction. It includes the bond-making and bond-breaking steps. This is a one-step reaction in which both nucleophile and substrate participate in the rate determining step.

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Students have asked these similar questions
(a) Under certain conditions, the reaction of 0.5 M 1-bromobutane with 1.0 M sodium methoxide forms 1-methoxybutane at arate of 0.05 mol>L per second. What would be the rate if 0.1 M 1-bromobutane and 2.0 M NaOCH3 were used?
The rate law for the reaction of HO- with tert-butyl bromide to form an elimination product in 75% ethanol/ 25% water at 30 °C is the sum of the rate laws for the E2 and E1 reactions. What percentage of the reaction takes place by an E2 pathway when [HO-] = 5.0 M? (k2 = 7.1 x 10-5, and k1 = 1.5 x 10-5)
What is the rate-determining step for an E1 reaction mechanism?

Chapter 6 Solutions

Organic Chemistry (9th Edition)

Ch. 6.7 - Prob. 6.11PCh. 6.7 - Prob. 6.12PCh. 6.8 - Prob. 6.13PCh. 6.9 - Predict the major products of the following...Ch. 6.9 - Prob. 6.15PCh. 6.10A - Prob. 6.16PCh. 6.11A - When diethyl ether (CH3CH2OCH2CH3) is treated with...Ch. 6.11B - Prob. 6.18PCh. 6.11B - For each pair of compounds, state which compound...Ch. 6.12 - Prob. 6.20PCh. 6.12 - Under appropriate conditions...Ch. 6.13 - Propose an SN1 mechanism for the solvolysis of...Ch. 6.13B - Prob. 6.23PCh. 6.13B - 3-Bromocyclohexene is a secondary halide, and...Ch. 6.15 - Prob. 6.25PCh. 6.15 - Prob. 6.26PCh. 6.16 - For each reaction, give the expected substitution...Ch. 6.16 - Prob. 6.28PCh. 6.16 - Prob. 6.29PCh. 6 - Prob. 6.30SPCh. 6 - Draw the structures of the following compounds. a....Ch. 6 - Give systematic (IUPAC) names for the following...Ch. 6 - Prob. 6.33SPCh. 6 - Predict the compound in each pair that will...Ch. 6 - Prob. 6.35SPCh. 6 - Give two syntheses for (CH3)2CHOCH2CH3, and...Ch. 6 - Prob. 6.37SPCh. 6 - Prob. 6.38SPCh. 6 - Chlorocyclohexane reacts with sodium cyanide...Ch. 6 - Give the substitution products expected from...Ch. 6 - Prob. 6.41SPCh. 6 - Prob. 6.42SPCh. 6 - Two of the carbocations in Problem6-42 are prone...Ch. 6 - Prob. 6.44SPCh. 6 - Predict the products of the following SN2...Ch. 6 - Prob. 6.46SPCh. 6 - Strawberry growers have used large quantities of...Ch. 6 - A solution of pure (S)-2-iodobutane ([]=+15.90) in...Ch. 6 - Prob. 6.49SPCh. 6 - Give a mechanism to explain the two products...Ch. 6 - Prob. 6.51SPCh. 6 - Because the SN1 reaction goes through a flat...Ch. 6 - Prob. 6.53SPCh. 6 - Furfuryl chloride can undergo substitution by both...Ch. 6 - Prob. 6.55SPCh. 6 - The following reaction takes place under...Ch. 6 - Propose mechanisms to account for the observed...Ch. 6 - Prob. 6.58SPCh. 6 - Prob. 6.59SP
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