EBK ORGANIC CHEMISTRY STUDY GUIDE AND S
EBK ORGANIC CHEMISTRY STUDY GUIDE AND S
6th Edition
ISBN: 9781319385415
Author: PARISE
Publisher: VST
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Chapter 10, Problem 10.33P
Interpretation Introduction

(a)

Interpretation:

The indicated groups are constitutionally equivalent or non-equivalent is to be identified. The indicated groups are to be classified as homotopic, enantiotopic, or diastereotopic when they are constitutionally equivalent.

Concept introduction:

The groups which are chemically nondistinguishable are termed as constitutionally equivalent. The groups which are chemically distinguishable are termed as constitutionally nonequivalent. The constitutionally equivalent groups can be further divided into three categories homotopic, enantiotopic, and diastereotopic.

Interpretation Introduction

(b)

Interpretation:

The indicated groups are constitutionally equilvalent or non-equivalent is to be identified. The indicated groups are to be classified as homotopic, enantiotopic, or diastereotopic when they are constitutionally equivalent.

Concept introduction:

The groups which are chemically nondistinguishable are termed as constitutionally equivalent. The groups which are chemically distinguishable are termed as constitutionally nonequivalent. The constitutionally equivalent groups can be further divided into three categories homotopic, enantiotopic, and diastereotopic.

Interpretation Introduction

(c)

Interpretation:

The indicated groups are constitutionally equivalent or non-equivalent is to be identified. The indicated groups are to be classified as homotopic, enantiotopic, or diastereotopic when they are constitutionally equivalent.

Concept introduction:

The groups which are chemically nondistinguishable are termed as constitutionally equivalent. The groups which are chemically distinguishable are termed as constitutionally nonequivalent. The constitutionally equivalent groups can be further divided into three categories homotopic, enantiotopic, and diastereotopic.

Interpretation Introduction

(d)

Interpretation:

The indicated groups are constitutionally equivalent or non-equivalent is to be identified. The indicated groups are to be classified as homotopic, enantiotopic, or diastereotopic when they are constitutionally equivalent.

Concept introduction:

The groups which are chemically nondistinguishable are termed as constitutionally equivalent. The groups which are chemically distinguishable are termed as constitutionally nonequivalent. The constitutionally equivalent groups can be further divided into three categories homotopic, enantiotopic, and diastereotopic.

Interpretation Introduction

(e)

Interpretation:

The indicated groups are constitutionally equivalent or non-equivalent is to be identified. The indicated groups are to be classified as homotopic, enantiotopic, or diastereotopic when they are constitutionally equivalent.

Concept introduction:

The groups which are chemically nondistinguishable are termed as constitutionally equivalent. The groups which are chemically distinguishable are termed as constitutionally nonequivalent. The constitutionally equivalent groups can be further divided into three categories homotopic, enantiotopic, and diastereotopic.

Interpretation Introduction

(f)

Interpretation:

The indicated hydrogen atoms and carbon -2 and carbon -4 are constitutionally equilvalent or non-equivalent is to be identified. The indicated groups are to be classified as homotopic, enantiotopic, or diastereotopic when they are constitutionally equivalent.

Concept introduction:

The groups which are chemically nondistinguishable are termed as constitutionally equivalent. The groups which are chemically distinguishable are termed as constitutionally nonequivalent. The constitutionally equivalent groups can be further divided into three categories homotopic, enantiotopic, and diastereotopic.

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I have a excitation/emission spectra of a quinine standard solution here, and I'm having trouble interpreting it. the red line is emission the blue line is excitation. i'm having trouble interpreting properly. just want to know if there is any evidence of raman or rayleigh peaks in the spectra.
Give the major product of the following reaction. excess 1. OH, H₂O 1.OH H CH3CH2CH21 H 2. A.-H₂O Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single bond is active by default.
2. Use Hess's law to calculate the AH (in kJ) for: rxn CIF(g) + F2(g) → CIF 3 (1) using the following information: 2CIF(g) + O2(g) → Cl₂O(g) + OF 2(g) AH = 167.5 kJ ΔΗ 2F2 (g) + O2(g) → 2 OF 2(g) 2C1F3 (1) + 202(g) → Cl₂O(g) + 3 OF 2(g) о = = -43.5 kJ AH = 394.1kJ

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EBK ORGANIC CHEMISTRY STUDY GUIDE AND S

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