ORGANIC CHEM PRINT STUDY GDE & SSM
ORGANIC CHEM PRINT STUDY GDE & SSM
4th Edition
ISBN: 9781119810650
Author: Klein
Publisher: WILEY
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Chapter 4, Problem 56PP
Interpretation Introduction

Interpretation:

The given conformations are needed to be ranked in order of increasing energy.

Concept introduction:

Conformations are arising due to the free rotation of CC bond. These rotations are measured by dihedral angle; it is the angle between two atoms attached to two different carbons of CC rotation in Newman projection.

The most and least energy occupied conformations are eclipsed and staggered, which are having a dihedral of ‘0’ and ‘60’ degree respectively.

Staggered conformation: conformation is said to be staggered when groups (attached to front and back carbons) are not aligned in the same axis.

ORGANIC CHEM PRINT STUDY GDE & SSM, Chapter 4, Problem 56PP , additional homework tip  1

Eclipsed conformation: conformation is said to be eclipsed when groups (attached to front and back carbons) are aligned in the same axis.

ORGANIC CHEM PRINT STUDY GDE & SSM, Chapter 4, Problem 56PP , additional homework tip  2

Because of the high torsional strain between atoms of eclipsed conformations, makes them more energized as compared to staggered conformations.

For eclipsed conformations, Torsional strain and steric interactions of atoms are the energizing factors.

For staggered conformations, anti-interactions and gauche interactions of atoms are the energizing factors.

To rank: the given conformations in order of increasing energy.

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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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