Organic Chemistry - Standalone book
Organic Chemistry - Standalone book
10th Edition
ISBN: 9780073511214
Author: Francis A Carey Dr., Robert M. Giuliano
Publisher: McGraw-Hill Education
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Chapter 5.3, Problem 5P
Interpretation Introduction

Interpretation:

The structural formulas are to be drawn for isomeric alcohols having molecular formula C4H10O and their functional class and substitutive names are to be written.

Concept introduction:

The molecular formula tells the number of atoms of each element present in the compound.

Each carbon atom forms four bonds while each oxygen atom forms two bonds. There are two pairs of unshared electrons on each oxygen atom.

The general formula for alcohol is ROH.

The isomers for alcohols can be drawn with the different possible connectivities of atoms.

For functional class nomenclature of alcohols, the numbering should be started from the carbon at which the hydroxyl group is attached and carbon chain should be named as alkyl group by adding “alcohol” as a separate word at the end.

For substitutive nomenclature of alcohols, the numbering should be given to the longest continuous chain having hydroxyl group in a way that the carbon bearing hydroxyl group should get the lowest number and the alcohol should be named by indicating the position of hydroxyl group by that carbon number and replacing “e” in the corresponding alkane by “ol.”

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Write out the structural formula for three ethers that have the formula C4H10O
2. Write bond-line structural formulas for (a.) two primary alcohols, (b.) a secondary alcohol, and (c.) atertiary alcohol—all having the molecular formula C4H10O.
3) Give the structural formulas and the old and new IUPAC names of all eight open-chain isomeric alcohols with the molecular formula CSH11OH. Indicate which of these isomers are primary, secondary, or tertiary alcohol. 4) Six isomeric saturated ethers have the molecular formula CsH120. Write the structural formula and name for each of these ethers.
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