The preparation of haloperidol compound has to be proposed. Concept Introduction: Retrosynthetic analysis: In an organic synthesis , the transformation of target molecule into simpler precursor molecules regardless of any reactivity or interaction with reagents. A retrosynthetic analysis is involving the breaking of a bond to form two or more synthons.

Question

For the reaction below: 1. Draw all reasonable elimination products to the right of the arrow. 2. In the box below the reaction, redraw any product you expect to be a major product. 田 Major Product: Check ☐ + I Na OH esc F1 F2 2 1 @ 2 Q W tab A caps lock S #3 80 F3 69 4 σ F4 % 95 S Click and drag to sta drawing a structure mm Save For Later 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use GO DII F5 F6 F7 F8 F9 F10 6 CO 89 & 7 LU E R T Y U 8* 9 0 D F G H J K L Z X C V B N M 36

Answer 1

Question

Chapter 22, Problem 22.61P

(a)

Interpretation Introduction

Interpretation:

The preparation of haloperidol compound has to be proposed.

Concept Introduction:

Retrosynthetic analysis:

In an organic synthesis, the transformation of target molecule into simpler precursor molecules regardless of any reactivity or interaction with reagents. A retrosynthetic analysis is involving the breaking of a bond to form two or more synthons.

(b)

Interpretation Introduction

Interpretation:

The chirality of haloperidol, and the possible of number of isomers in the given synthesis has to be given.

Concept Introduction:

Stereoisomers and chiral:

Isomers differing only in their spatial arrangement of atoms are called as stereoisomers.

The geometric property of a molecule that cannot be superimposed on its mirror image is known as chirality. Chiral carbon is the one which is attached with four different groups or atoms.

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