IUPAC name for the given aldehyde has to be chosen from the given options. Concept Introduction: For naming an aldehyde in IUPAC nomenclature , the suffix “-al” is added to the parent alkane name. IUPAC rules for naming an aldehyde: The longest parent carbon chain is identified that includes the carbonyl group. The parent chain name is changed by replacing the suffix “-e” with “-al”. Numbering is done in a way that the carbonyl group is designated as number 1. This is not indicated in the part of the name because for aldehyde, the carbonyl carbon is always numbered 1. The identity and location of substituents if any has to be determined and this information has to be added in front of the IUPAC name. If the carbonyl functional group is attached to a ring of carbon atoms, the ring is named and “-carbaldehyde” is added as suffix.

Question

You are trying to decide if there is a single reagent you can add that will make the following synthesis possible without any other major side products: xi 1. ☑ 2. H₂O хе i Draw the missing reagent X you think will make this synthesis work in the drawing area below. If there is no reagent that will make your desired product in good yield or without complications, just check the box under the drawing area and leave it blank. Click and drag to start drawing a structure. There is no reagent that will make this synthesis work without complications. : ☐ S ☐

Answer 1

Question

Chapter 4.4, Problem 1QQ

Interpretation Introduction

Interpretation:

IUPAC name for the given aldehyde has to be chosen from the given options.

Concept Introduction:

For naming an aldehyde in IUPAC nomenclature, the suffix “-al” is added to the parent alkane name.

IUPAC rules for naming an aldehyde:

The longest parent carbon chain is identified that includes the carbonyl group.

The parent chain name is changed by replacing the suffix “-e” with “-al”.

Numbering is done in a way that the carbonyl group is designated as number 1. This is not indicated in the part of the name because for aldehyde, the carbonyl carbon is always numbered 1.

The identity and location of substituents if any has to be determined and this information has to be added in front of the IUPAC name.

If the carbonyl functional group is attached to a ring of carbon atoms, the ring is named and “-carbaldehyde” is added as suffix.

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