ORGANIC CHEMISTRY-W/S.G+SOLN.MANUAL
ORGANIC CHEMISTRY-W/S.G+SOLN.MANUAL
8th Edition
ISBN: 9780134595450
Author: Bruice
Publisher: PEARSON
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Chapter 20.10, Problem 20P

a)

Interpretation Introduction

Interpretation:

The structure of the given sugar β-D-galactopyranose is to be drawn by using Haworth projections.

Concept Introduction:

Haworth projections are used to represent the cyclic structures of the monosaccharides. In other words,

“A common way of writing a structural formula to represent the cyclic structure of monosaccharide with a simple three-dimensional perspective is called Haworth projection”.

b)

Interpretation Introduction

Interpretation:

The structure of the given sugar α-D-tagatopyranose is to be drawn by using Haworth projections.

Concept Introduction:

Haworth projections are used to represent the cyclic structures of the monosaccharides. In other words,

“A common way of writing a structural formula to represent the cyclic structure of monosaccharide with a simple three-dimensional perspective is called Haworth projection”.

c)

Interpretation Introduction

Interpretation: The structure of the given sugar α-D-tagatopyranose is to be drawn by using Haworth projections.

Concept Introduction:

Haworth projections are used to represent the cyclic structures of the monosaccharides. In other words,

“A common way of writing a structural formula to represent the cyclic structure of monosaccharide with a simple three-dimensional perspective is called Haworth projection”.

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1. a) Assuming that an atom of arsenic has hydrogen-like atomic orbitals, sketch the radial probability plots for 4p and 4d orbitals of S atom. Indicate angular and radial nodes in these orbitals. (4 points) b) Calculate Zeff experienced by and electron in 4p AO's in a arsenic atom. Use Slater rules that were discussed in lecture. (3 points)
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ORGANIC CHEMISTRY-W/S.G+SOLN.MANUAL

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