EBK ORGANIC CHEMISTRY: PRINCIPLES AND M
EBK ORGANIC CHEMISTRY: PRINCIPLES AND M
2nd Edition
ISBN: 9780393630817
Author: KARTY
Publisher: W.W.NORTON+CO. (CC)
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Chapter E, Problem E.28P
Interpretation Introduction

(a)

Interpretation:

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

Concept introduction:

To write the IUPAC name, first it is important to determine the highest-priority functional group present that requires a suffix referring to Table E-1. In the molecule that contains both, an OH and a NH2 functional group, the functional group OH gets priority over NH2 functional group, and -ol is added as a suffix to the IUPAC name. Next, the main chain or ring containing the highest-priority functional group is to be determined. The next step is to number the main chain or ring such that carbon atoms involving the highest-priority functional group receive the lowest possible numbers. The locator number for the highest-priority functional group is written immediately before the suffix, unless needed. All other functional groups in the molecule are treated as substituents and appear in the name as a prefix. Prefixes such as ‘di’, ‘tri’, ‘tetra’... etc. are used to indicate the number of identical substituents attached. The substituents are written in the alphabetical order.

Interpretation Introduction

(b)

Interpretation:

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

Concept introduction:

To write the IUPAC name, first it is important to determine the highest-priority functional group present that requires a suffix referring to Table E-1. The molecule that contains both, an OH and a NH2 functional group, the functional group OH gets priority over NH2 functional group, and the -ol is added as a suffix to the IUPAC name. Next, the main chain or ring containing the highest-priority functional group is to be determined. The next step is to number the main chain or ring such that carbon atoms involving the highest-priority functional group receive the lowest possible numbers. The locator number for the highest-priority functional group is written immediately before the suffix, unless needed. All other functional groups in the molecule are treated as substituents and appear in the name as a prefix. Prefixes like ‘di’, ‘tri’, ‘tetra’… etc. are used to indicate the number of identical substituents attached. The substituents are written in the alphabetical order.

Interpretation Introduction

(c)

Interpretation:

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

Concept introduction:

To write the IUPAC name, first it is important to determine the highest-priority functional group present that requires a suffix referring to Table E-1. The molecule that contains both, an OH and a NH2 functional group, the functional group OH gets priority over NH2 functional group, and the -ol is added as a suffix to the IUPAC name. Next, the main chain or ring containing the highest-priority functional group is to be determined. The next step is to number the main chain or ring such that carbon atoms involving the highest-priority functional group receive the lowest possible numbers. The locator number for the highest-priority functional group is written immediately before the suffix, unless needed. All other functional groups in the molecule are treated as substituents and appear in the name as a prefix. Prefixes such as ‘di’, ‘tri’, ‘tetra’... etc. are used to indicate the number of identical substituents attached. The substituents are written in the alphabetical order.

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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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