ORGANIC CHEMISTRY 1 TERM ACCESS
ORGANIC CHEMISTRY 1 TERM ACCESS
3rd Edition
ISBN: 9781119661511
Author: Klein
Publisher: WILEY
Question
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Chapter 19.5, Problem 9ATS

(a)

Interpretation Introduction

Interpretation: The reagents and conditions that are required for the given transformation have to be determined.

Concept Introduction:

Acetals:

Acetals are used to protect the ketone and aldehyde (carbonyl group).

In this reaction acetone is protected as acetal by using ethylene glycol. Acetals are less stable compound.

ORGANIC CHEMISTRY 1 TERM ACCESS, Chapter 19.5, Problem 9ATS , additional homework tip  1

In acidic condition, an aldehyde or a ketone reacts with two molecules of alcohol or a molecule of diol to form acetal or cyclic acetal respectively.

General scheme:

ORGANIC CHEMISTRY 1 TERM ACCESS, Chapter 19.5, Problem 9ATS , additional homework tip  2

Retro synthetic analysis:

It is the analysis of the synthetic starting materials for a given compound through its precursors or fragments which are known as synthons. The synthons can be obtained by logical cleavage of the chemical bonds in the compounds. The resulted synthons will be therefore known as logical synthons.

Retro analysis for acetal formation:

The retro synthetic analysis for any given acetal, enable to find that the starting materials for its formation will be alcohol in case of aliphatic acetal or diol in case of cyclic acetal as well as aldehyde or ketone.

Example:

The retro analysis for a cyclic acetal is shown here:

ORGANIC CHEMISTRY 1 TERM ACCESS, Chapter 19.5, Problem 9ATS , additional homework tip  3

The given retro analysis shows that the starting materials for the formation of the acetal are a diol and formaldehyde.

General scheme:

ORGANIC CHEMISTRY 1 TERM ACCESS, Chapter 19.5, Problem 9ATS , additional homework tip  4

(b)

Interpretation Introduction

Interpretation: A plausible mechanism for the given reaction has to be drawn.

Concept Introduction:

Acetals:

Acetals are used to protect the ketone and aldehyde (carbonyl group).

In this reaction acetone is protected as acetal by using ethylene glycol. Acetals are less stable compound.

ORGANIC CHEMISTRY 1 TERM ACCESS, Chapter 19.5, Problem 9ATS , additional homework tip  5

In acidic condition, an aldehyde or a ketone reacts with two molecules of alcohol or a molecule of diol to form acetal or cyclic acetal respectively.

General scheme:

ORGANIC CHEMISTRY 1 TERM ACCESS, Chapter 19.5, Problem 9ATS , additional homework tip  6

(c)

Interpretation Introduction

Interpretation: Based on the given keto-diol precursor, the structure of frontalin has to be drawn.

Concept Introduction:

Acetals:

Acetals are used to protect the ketone and aldehyde (carbonyl group).

In this reaction acetone is protected as acetal by using ethylene glycol. Acetals are less stable compound.

ORGANIC CHEMISTRY 1 TERM ACCESS, Chapter 19.5, Problem 9ATS , additional homework tip  7

In acidic condition, an aldehyde or a ketone reacts with two molecules of alcohol or a molecule of diol to form acetal or cyclic acetal respectively.

General scheme:

ORGANIC CHEMISTRY 1 TERM ACCESS, Chapter 19.5, Problem 9ATS , additional homework tip  8

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Provide the unknown for the given data.
Electron Arrangement A. Fill in the following chart relating to levels, sublevels and orbitals. Levels (n) 1 Sublevels # of Orbitals per sublevel 2 3 4 # of Electrons per sublevel Total Electrons per level Complete: B. Answer the following questions related to levels, sublevels, orbitals and electrons. 1. How many sublevels are in energy level 2? 2. How many orbitals are in a 4f sublevel? 3. How many electrons can level 3 hold? 4. How many orbitals are in level 4? 5. How many electrons can sublevel 2p hold? 11
Provide the unknown for the given details.

Chapter 19 Solutions

ORGANIC CHEMISTRY 1 TERM ACCESS

Ch. 19.5 - Prob. 9ATSCh. 19.5 - Prob. 10CCCh. 19.5 - Prob. 11CCCh. 19.5 - Prob. 12CCCh. 19.5 - Prob. 13CCCh. 19.6 - Prob. 3LTSCh. 19.6 - Prob. 14PTSCh. 19.6 - Prob. 15PTSCh. 19.6 - Prob. 16ATSCh. 19.6 - Prob. 17CCCh. 19.6 - Prob. 18CCCh. 19.6 - Prob. 20PTSCh. 19.6 - Prob. 21ATSCh. 19.6 - Prob. 22CCCh. 19.7 - Prob. 5LTSCh. 19.7 - Prob. 23PTSCh. 19.7 - Prob. 24ATSCh. 19.7 - Prob. 25CCCh. 19.8 - Prob. 26CCCh. 19.8 - Prob. 27CCCh. 19.9 - Prob. 28CCCh. 19.9 - Prob. 29CCCh. 19.10 - Prob. 30CCCh. 19.10 - Prob. 31CCCh. 19.10 - Prob. 32CCCh. 19.10 - Prob. 33CCCh. 19.10 - Prob. 6LTSCh. 19.10 - Prob. 34PTSCh. 19.10 - Prob. 35PTSCh. 19.10 - Prob. 36ATSCh. 19.10 - Prob. 37ATSCh. 19.10 - Prob. 38CCCh. 19.11 - Prob. 39CCCh. 19.12 - Prob. 7LTSCh. 19.12 - Prob. 40PTSCh. 19.12 - Prob. 41ATSCh. 19.13 - Prob. 42CCCh. 19 - Prob. 43PPCh. 19 - Prob. 44PPCh. 19 - Prob. 45PPCh. 19 - Prob. 46PPCh. 19 - Prob. 47PPCh. 19 - Prob. 48PPCh. 19 - Prob. 49PPCh. 19 - Prob. 50PPCh. 19 - Prob. 51PPCh. 19 - Prob. 52PPCh. 19 - Prob. 53PPCh. 19 - Prob. 54PPCh. 19 - Prob. 55PPCh. 19 - Prob. 56PPCh. 19 - Prob. 57PPCh. 19 - Prob. 58PPCh. 19 - Prob. 59PPCh. 19 - Prob. 60PPCh. 19 - Predict the major product(s) obtained when each of...Ch. 19 - Prob. 62PPCh. 19 - Prob. 63PPCh. 19 - Prob. 64PPCh. 19 - Prob. 65PPCh. 19 - Prob. 66PPCh. 19 - Prob. 67PPCh. 19 - Prob. 68PPCh. 19 - Prob. 69PPCh. 19 - Prob. 70PPCh. 19 - Prob. 71PPCh. 19 - Prob. 72PPCh. 19 - Prob. 73PPCh. 19 - Prob. 74IPCh. 19 - Prob. 75IPCh. 19 - Prob. 76IPCh. 19 - Prob. 77IPCh. 19 - Prob. 78IPCh. 19 - Prob. 79IPCh. 19 - Prob. 80IPCh. 19 - Prob. 81IPCh. 19 - Prob. 83IPCh. 19 - Prob. 84IPCh. 19 - Prob. 85IPCh. 19 - Prob. 86IPCh. 19 - Prob. 87IPCh. 19 - Prob. 88IPCh. 19 - Prob. 89IPCh. 19 - Prob. 90IPCh. 19 - Prob. 91IPCh. 19 - Prob. 92IPCh. 19 - Prob. 93IPCh. 19 - Prob. 94CPCh. 19 - Prob. 95CPCh. 19 - Treatment of the following ketone with LiAIHa...
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