EBK ORGANIC CHEMISTRY: PRINCIPLES AND M
EBK ORGANIC CHEMISTRY: PRINCIPLES AND M
2nd Edition
ISBN: 9780393543971
Author: KARTY
Publisher: VST
Question
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Chapter E, Problem E.39P
Interpretation Introduction

(a)

Interpretation:

For the given corresponding molecule, the IUPAC name is to be written.

Concept introduction:

The name of a compound, other than those containing only a double or a triple bond, halogen, nitro group, and ether, is made up of three parts. A prefix shows the presence of additional functional groups like halo, nitro, etc. The root name indicates the number of carbon atoms in the longest chain, along with the presence and position of C=C and CC if present. Finally, a suffix corresponding to the highest priority group replaces the ‘e’ in the alkane/alkene/alkyne root name along with its position indicator. The position indicator (locant) may be dropped if redundant. An exception to replacing the ‘e’ is nitriles. All other groups, of lower priority, are treated as substituents and appear in the prefix. In case of aldehydes and ketone, if the carbonyl carbon is in the longest chain of carbon atoms, it is also counted toward its length.

Interpretation Introduction

(b)

Interpretation:

For the given corresponding molecule, the IUPAC name is to be written.

Concept introduction:

The name of a compound, other than those containing only a double or a triple bond, halogen, nitro group, and ether, is made up of three parts. A prefix shows the presence of additional functional groups like halo, nitro, etc. The root name indicates the number of carbon atoms in the longest chain, along with the presence and position of C=C and CC if present. Finally, a suffix corresponding to the highest priority group replaces the ‘e’ in the alkane/alkene/alkyne root name along with its position indicator. An exception to replacing the ‘e’ is nitriles. All other groups, of lower priority, are treated as substituents and appear in the prefix. In case of aldehydes and ketone, if the carbonyl carbon is in the longest chain of carbon atoms, it is also counted toward its length.

Interpretation Introduction

(c)

Interpretation:

For the given corresponding molecule, the IUPAC name is to be written.

Concept introduction:

The name of a compound, other than those containing only a double or a triple bond, halogen, nitro group and ether, is made up of three parts. A prefix shows the presence of additional functional groups like halo, nitro, etc. The root name indicates the number of carbon atoms in the longest chain, along with the presence and position of C=C and CC if present. Finally, a suffix corresponding to the highest priority group replaces the ‘e’ in the alkane/alkene/alkyne root name along with its position indicator. An exception to replacing the ‘e’ is nitriles. All other groups, of lower priority, are treated as substituents and appear in the prefix. In case of aldehydes and ketone, if the carbonyl carbon is in the longest chain of carbon atoms, it is also counted toward its length.

Interpretation Introduction

(d)

Interpretation:

The molecule corresponding to the given IUPAC name is to be drawn.

Concept introduction:

The name of a compound other than those containing only a double or a triple bond, halogen, nitro group and ether, is made up of three parts. A prefix shows the presence of additional functional groups like halo, nitro, etc. The root name indicates the number of carbon atoms in the longest chain, along with the presence and position of C=C and CC if present. Finally, a suffix corresponding to the highest priority group replaces the ‘e’ in the alkane/alkene/alkyne root name along with its position indicator. An exception to replacing the ‘e’ is nitriles. All other groups, of lower priority, are treated as substituents and appear in the prefix. In case of aldehydes and ketone, if the carbonyl carbon is in the longest chain of carbon atoms, it is also counted toward its length.

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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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