ORG CHEM W/ EBOOK & SW5 + STUDY GUIDE
ORG CHEM W/ EBOOK & SW5 + STUDY GUIDE
2nd Edition
ISBN: 9780393666144
Author: KARTY
Publisher: NORTON
Question
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Chapter F, Problem F.14P
Interpretation Introduction

(a)

Interpretation:

For the given carboxylic acid, the IUPAC name is to be determined.

Concept introduction:

While naming a carboxylic acid, following basic rules are used.

Select the longest possible carbon root chain that contains the acid functional group ( CO2). The numbering begins at carbonyl carbon of acid functional group. If there is only one acid group, then the suffix is oic acid. If two acid groups are present, then the chain that contains carbonyl carbons of both groups is treated as the root, and the suffix used is dioic acid.

Any other substituents are listed alphabetically as prefixes along with their locants.

Interpretation Introduction

(b)

Interpretation:

For the given carboxylic acid, the IUPAC name is to be determined.

Concept introduction:

Following are the basic rules are used while naming a carboxylic acid.

Select the longest possible carbon root chain that contains the acid functional group ( CO2). The numbering begins at carbonyl carbon of acid functional group. If there is only one acid group, then the suffix is oic acid. If two acid groups are present, then the chain that contains carbonyl carbons of both groups is treated as the root, and the suffix used is dioic acid.

Any other substituents are listed alphabetically as prefixes along with their locants.

Interpretation Introduction

(c)

Interpretation:

For the given carboxylic acid, the IUPAC name is to be determined.

Concept introduction:

Following are the basic rules are used while naming a carboxylic acid.

Select the longest possible carbon root chain that contains the acid functional group ( CO2). The numbering begins at carbonyl carbon of acid functional group. If there is only one acid group, then the suffix is oic acid. If two acid groups are present, then the chain that contains carbonyl carbons of both groups is treated as the root, and the suffix used is dioic acid.

Any other substituents are listed alphabetically as prefixes along with their locants.

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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."
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