The product obtained in Practice Problem 12.4 as primary, secondary, or tertiary alcohol has to be classified and common name and IUPAC name has to be given. Concept Introduction: A common nomenclature of naming organic compounds has been developed by IUPAC. By usage of this nomenclature or rules, memorizing of names of organic compounds is not necessary. IUPAC rules for naming alcohols: Alcohols are named by identifying the parent compound and replacing the –e ending with –ol . Lowest possible number should be given for the hydroxyl group present in the parent chain. Name and number all substituent, and put them as prefixes to “ alkanol ” name also give the first preference as per the alphabetical order. If an alcohol contains two hydroxyl groups then name it as diol , an alcohol; contains three hydroxyl groups then name it as triol . Common names for alcohols are derived from alkyl group corresponding to the parent compound.

Question

Want to see the full answer?

Answer 1

Question

Chapter 12.4, Problem 12.3Q

Interpretation Introduction

Interpretation:

The product obtained in Practice Problem 12.4 as primary, secondary, or tertiary alcohol has to be classified and common name and IUPAC name has to be given.

Concept Introduction:

A common nomenclature of naming organic compounds has been developed by IUPAC. By usage of this nomenclature or rules, memorizing of names of organic compounds is not necessary.

IUPAC rules for naming alcohols:

Alcohols are named by identifying the parent compound and replacing the –e ending with –ol.

Lowest possible number should be given for the hydroxyl group present in the parent chain.

Name and number all substituent, and put them as prefixes to “alkanol” name also give the first preference as per the alphabetical order.

If an alcohol contains two hydroxyl groups then name it as diol, an alcohol; contains three hydroxyl groups then name it as triol.

Common names for alcohols are derived from alkyl group corresponding to the parent compound.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

Draw the Fischer projection of D-fructose. Click and drag to start drawing a structure. Skip Part Check AP 14 tv SC F1 F2 80 F3 a F4 ! 2 # 3 CF F5 75 Ax MacBook Air 894 $ 5olo % Λ 6 > W F6 K F7 &

Consider this step in a radical reaction: Y What type of step is this? Check all that apply. Draw the products of the step on the right-hand side of the drawing area below. If more than one set of products is possible, draw any set. Also, draw the mechanism arrows on the left-hand side of the drawing area to show how this happens. ionization propagation initialization passivation none of the above

22.16 The following groups are ortho-para directors. (a) -C=CH₂ H (d) -Br (b) -NH2 (c) -OCHS Draw a contributing structure for the resonance-stabilized cation formed during elec- trophilic aromatic substitution that shows the role of each group in stabilizing the intermediate by further delocalizing its positive charge. 22.17 Predict the major product or products from treatment of each compound with Cl₁/FeCl₂- OH (b) NO2 CHO 22.18 How do you account for the fact that phenyl acetate is less reactive toward electro- philic aromatic substitution than anisole? Phenyl acetate Anisole CH (d)