Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second)
Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second)
2nd Edition
ISBN: 9780393655551
Author: KARTY, Joel
Publisher: W. W. Norton & Company
Question
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Chapter A, Problem A.24P
Interpretation Introduction

(a)

Interpretation:

The structure from the provided IUPAC name is to be drawn.

Concept introduction:

The last part of the IUPAC name represents, the parent chain which is the longest continuous carbon chain. The names of all substituents appear as prefixes before the root, and they are appear alphabetically according to the substituent’s name. If there is just one of a particular substituent, the locator number appears immediately to the left of the substituent it describes. The prefixes, ‘di, tri... ’ suggests the number of substituents present along the parent chain. The locator numbers of substituents represents the carbon atoms in the parent chain to which the substituents are attached. A parenthesis represents a substituted branched alkane, while the number just before the parenthesis denotes the point of attachment of the substituted branched alkane to the parent chain.

Interpretation Introduction

(b)

Interpretation:

The structure from the given IUPAC name is to be drawn.

Concept introduction:

The last part of the IUPAC name represents the parent chain which is the longest continuous carbon chain. The names of all substituents appear as prefixes before the root, and they appear alphabetically according to the substituent’s name. If there is just one of a particular substituent, the locator number appears immediately to the left of the substituent it describes. The prefixes, ‘di, tri’ suggests the number of substituents present along the parent chain. The locator numbers of substituents represent the carbon atoms in the parent chain to which the substituents are attached. A parenthesis represents a substituted branched alkane, while the number just before the parenthesis denotes the point of attachment of the substituted branched alkane to the parent chain.

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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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