Get Ready for Organic Chemistry
Get Ready for Organic Chemistry
2nd Edition
ISBN: 9780321774125
Author: KARTY, Joel
Publisher: PEARSON
Question
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Chapter 19, Problem 19.55P
Interpretation Introduction

(a)

Interpretation:

How to carry out the given transformation is to be shown.

Concept introduction:

The C=C functional group of an alkene or the CC functional group of an alkyne can be removed via catalytic hydrogenation. Catalytic hydrogenation is a reaction in which H2 adds to a molecule in the presence of a metal catalyst such as Pt, Pd, or Ni. Catalytic hydrogenation readily reduces an alkene or an alkyne to an alkane. The reduction of an alkyne to an alkene via catalytic hydrogenation favors production of the cis isomer over the trans. Catalytic hydrogenation using a poisoned catalyst (a Lindlar catalyst) reduces an alkyne to a cis alkene. The functional groups in alkenes, alkynes, and aldehydes can be selectively reduced over those in ketones, nitriles, and amides.

Interpretation Introduction

(b)

Interpretation:

How to carry out the given transformation is to be shown.

Concept introduction:

The C=C functional group of an alkene or the CC functional group of an alkyne can be removed via catalytic hydrogenation. Catalytic hydrogenation is a reaction in which H2 adds to a molecule in the presence of a metal catalyst such as Pt, Pd, or Ni. Catalytic hydrogenation readily reduces an alkene or an alkyne to an alkane. The reduction of an alkyne to an alkene via catalytic hydrogenation favors production of the cis isomer over the trans. Catalytic hydrogenation using a poisoned catalyst (a Lindlar catalyst) reduces an alkyne to a cis alkene. The functional groups in alkenes, alkynes, and aldehydes can be selectively reduced over those in ketones, nitriles, and amides.

Interpretation Introduction

(c)

Interpretation:

How to carry out the given transformation is to be shown.

Concept introduction:

The C=C functional group of an alkene or the CC functional group of an alkyne can be removed via catalytic hydrogenation. Catalytic hydrogenation is a reaction in which H2 adds to a molecule in the presence of a metal catalyst such as Pt, Pd, or Ni. Catalytic hydrogenation readily reduces an alkene or an alkyne to an alkane. The reduction of an alkyne to an alkene via catalytic hydrogenation favors production of the cis isomer over the trans. Catalytic hydrogenation using a poisoned catalyst (a Lindlar catalyst) reduces an alkyne to a cis alkene. The functional groups in alkenes, alkynes, and aldehydes can be selectively reduced over those in ketones, nitriles, and amides.

Interpretation Introduction

(d)

Interpretation:

How to carry out the given transformation is to be shown.

Concept introduction:

The C=C functional group of an alkene or the CC functional group of an alkyne can be removed via catalytic hydrogenation. Catalytic hydrogenation is a reaction in which H2 adds to a molecule in the presence of a metal catalyst such as Pt, Pd, or Ni. Catalytic hydrogenation readily reduces an alkene or an alkyne to an alkane. The reduction of an alkyne to an alkene via catalytic hydrogenation favors production of the cis isomer over the trans. Catalytic hydrogenation using a poisoned catalyst (a Lindlar catalyst) reduces an alkyne to a cis alkene. The functional groups in alkenes, alkynes, and aldehydes can be selectively reduced over those in ketones, nitriles, and amides.

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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 19 Solutions

Get Ready for Organic Chemistry

Ch. 19 - Prob. 19.11PCh. 19 - Prob. 19.12PCh. 19 - Prob. 19.13PCh. 19 - Prob. 19.14PCh. 19 - Prob. 19.15PCh. 19 - Prob. 19.16PCh. 19 - Prob. 19.17PCh. 19 - Prob. 19.18PCh. 19 - Prob. 19.19PCh. 19 - Prob. 19.20PCh. 19 - Prob. 19.21PCh. 19 - Prob. 19.22PCh. 19 - Prob. 19.23PCh. 19 - Prob. 19.24PCh. 19 - Prob. 19.25PCh. 19 - Prob. 19.26PCh. 19 - Prob. 19.27PCh. 19 - Prob. 19.28PCh. 19 - Prob. 19.29PCh. 19 - Prob. 19.30PCh. 19 - Prob. 19.31PCh. 19 - Prob. 19.32PCh. 19 - Prob. 19.33PCh. 19 - Prob. 19.34PCh. 19 - Prob. 19.35PCh. 19 - Prob. 19.36PCh. 19 - Prob. 19.37PCh. 19 - Prob. 19.38PCh. 19 - Prob. 19.39PCh. 19 - Prob. 19.40PCh. 19 - Prob. 19.41PCh. 19 - Prob. 19.42PCh. 19 - Prob. 19.43PCh. 19 - Prob. 19.44PCh. 19 - Prob. 19.45PCh. 19 - Prob. 19.46PCh. 19 - Prob. 19.47PCh. 19 - Prob. 19.48PCh. 19 - Prob. 19.49PCh. 19 - Prob. 19.50PCh. 19 - Prob. 19.51PCh. 19 - Prob. 19.52PCh. 19 - Prob. 19.53PCh. 19 - Prob. 19.54PCh. 19 - Prob. 19.55PCh. 19 - Prob. 19.56PCh. 19 - Prob. 19.57PCh. 19 - Prob. 19.58PCh. 19 - Prob. 19.59PCh. 19 - Prob. 19.60PCh. 19 - Prob. 19.61PCh. 19 - Prob. 19.62PCh. 19 - Prob. 19.63PCh. 19 - Prob. 19.64PCh. 19 - Prob. 19.65PCh. 19 - Prob. 19.66PCh. 19 - Prob. 19.67PCh. 19 - Prob. 19.68PCh. 19 - Prob. 19.69PCh. 19 - Prob. 19.70PCh. 19 - Prob. 19.71PCh. 19 - Prob. 19.72PCh. 19 - Prob. 19.73PCh. 19 - Prob. 19.74PCh. 19 - Prob. 19.75PCh. 19 - Prob. 19.76PCh. 19 - Prob. 19.77PCh. 19 - Prob. 19.78PCh. 19 - Prob. 19.79PCh. 19 - Prob. 19.1YTCh. 19 - Prob. 19.2YTCh. 19 - Prob. 19.3YTCh. 19 - Prob. 19.4YTCh. 19 - Prob. 19.5YTCh. 19 - Prob. 19.6YTCh. 19 - Prob. 19.7YTCh. 19 - Prob. 19.8YTCh. 19 - Prob. 19.9YTCh. 19 - Prob. 19.10YT
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