Organic Chemistry
Organic Chemistry
2nd Edition
ISBN: 9781118452288
Author: David R. Klein
Publisher: WILEY
Question
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Chapter 7, Problem 43PP

(a)

Interpretation Introduction

Interpretation: The rate for the given reaction should be analyzed for the given condition.

Concept Introduction:

SN1 Reaction: it is a nucleophilic substitution reaction in which the rate determining step depends on one reactant. First step is the formation of more stable carbocation which is followed by the attack of nucleophile.

The rate of SN1 depends only on the formation of the more stable carbocation present in the substrate. The reactivity increases with better leaving group in the substrate. It does not depends on the nucleophile present.

Carbocation: carbon ion that bears a positive charge on it.

Leaving group: it is a fragment that leaves a substrate in a chemical reaction with a pair of electrons via heterolytic bond cleavage.

Polar protic solvent: solvents that contains H+ which is directly bonded to electronegative atom.

Electronegativity: it is the tendency of atoms to attract a lone pair of electrons towards itself in a substrate. Electronegativity property follows the trend that it increases across periods and decreases down the column in the periodic table.

Nucleophile - negatively charged species which donates electron pairs. Eg. Cl- , Br- etc.,

(b)

Interpretation Introduction

Interpretation: The rate for the given reaction should be analyzed for the given condition.

Concept Introduction:

SN1 Reaction: it is a nucleophilic substitution reaction in which the rate determining step depends on one reactant. First step is the formation of more stable carbocation which is followed by the attack of nucleophile.

The rate of SN1 depends only on the formation of the more stable carbocation present in the substrate. The reactivity increases with better leaving group in the substrate. It does not depends on the nucleophile present.

Carbocation: carbon ion that bears a positive charge on it.

Leaving group: it is a fragment that leaves a substrate in a chemical reaction with a pair of electrons via heterolytic bond cleavage.

Polar protic solvent: solvents that contains H+ which is directly bonded to electronegative atom.

Electronegativity: it is the tendency of atoms to attract a lone pair of electrons towards itself in a substrate. Electronegativity property follows the trend that it increases across periods and decreases down the column in the periodic table.

Nucleophile - negatively charged species which donates electron pairs. Eg. Cl- , Br- etc.,

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#1. Retro-Electrochemical Reaction: A ring has been made, but the light is causing the molecule to un- cyclize. Undo the ring into all possible molecules. (2pts, no partial credit) hv
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I have a question about this problem involving mechanisms and drawing curved arrows for acids and bases. I know we need to identify the nucleophile and electrophile, but are there different types of reactions? For instance, what about Grignard reagents and other types that I might not be familiar with? Can you help me with this? I want to identify the names of the mechanisms for problems 1-14, such as Gilman reagents and others. Are they all the same? Also, could you rewrite it so I can better understand? The handwriting is pretty cluttered. Additionally, I need to label the nucleophile and electrophile, but my main concern is whether those reactions differ, like the "Brønsted-Lowry acid-base mechanism, Lewis acid-base mechanism, acid-catalyzed mechanisms, acid-catalyzed reactions, base-catalyzed reactions, nucleophilic substitution mechanisms (SN1 and SN2), elimination reactions (E1 and E2), organometallic mechanisms, and so forth."

Chapter 7 Solutions

Organic Chemistry

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