How would you synthesize the following alcohols, starting with benzene and other alcohols of six or fewer carbons as your only organic reagents?

(a)

(b)

(c)

(d)

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(a)

(b)

(c)

(d)

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01

Synthesis of alcohols

The hydration of alkenes and the reduction of aldehydes, ketones, acids and esters leads to the formation of alcohols. The hydrolysis of halides can also generate alcohols. The hydroboration of alkenes can also generate alcohols.

02

Synthesizing the alcohol starting with other alcohols

(a)In this reaction, ethanol reacts with PBr3to form ethyl bromide. This product further reacts with Mg and ether to form ethyl magnesium bromide. This is the Grignard reagent used for the reaction.

Cyclohexanol reacts with CrO3and H3O+to form cyclohexanone. This further reacts with ethyl magnesium bromide and localid="1656436210972" H3O+to form the given compound 1-ethylcyclohexanol. The reaction can be given as:

Reaction (a)

(b)In this reaction, 2-methylpentan-1-ol reacts with localid="1656436216714" PBr3to form 1-bromo-2-methylpentane. This further reacts with Mg and ether to form (2-methylpentyl) magnesium bromide. This is used as the Grignard reagent.

Methanol reacts with Periodinane and localid="1656436223461" CH2Cl2to form formaldehyde. This further reacts with the Grignard reagent formed above in the presence of ether and localid="1656436229512" H3O+to form 3-methyl-hexan-1-ol. The reaction can be given as:

Reaction (b)

(c)Benzene reacts with Br2and FeBr3to form bromobenzene. This further reacts with Mg and ether to form phenyl magnesium bromide.

The alcohol, pentan-2-ol reacts with localid="1656436235665" CrO3and localid="1656436241025" H3O+to form pentan-2-one.

Phenyl magnesium bromide reacts with pentan-2-one in the presence of ether and localid="1656436246376" H3O+to form the compound 2-phenyl-pentan-2-ol. The reaction can be given as:

(d)The Grignard reagent used in this reaction is ethyl magnesium bromide.

The compound, 3-methylbutan-1-ol reacts with periodinane and localid="1656436292646" CH2CI2to form 3-methylbutanal. This compound reacts with ethyl magnesium bromide in the presence of ether and localid="1656436305787" H3O+to form 5-methylhexan-3-ol. The reaction can be given as:

Reaction (d)

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Most popular questions from this chapter

Propose structures for alcohols that have the following H1 NMR spectra:

(a) C5H12O

(b) C8H10O

A compound of unknown structure gave the following spectroscopic data:

Mass spectrum:M+=88.1

IR: 3600cm-1

1HNMR: 1.4δ (2H, quartet, J=7Hz); 1.2δ (6H, singlet); 1.0δ (1H, singlet); 0.9δ (3H, triplet, J=7Hz)

13CNMR: 74, 35, 27, 25δ

(a) Assuming that the compound contains C and H but may or may not contain O, give three possible molecular formulas.

(b) How many protons (H) does the compound contain?

(c) What functional group(s) does the compound contain?

(d) How many carbons does the compound contain?

(e) What is the molecular formula of the compound?

(f) What is the structure of the compound?

(g) Assign peaks in the molecule’s NMR spectrum corresponding to specific protons.

Question:Which of the eight alcohols that you identified in Problem 17-38 react with CrO3 in aqueous acid? Show the products you would expect from each reaction

Compound A, C5H10O, is one of the basic building blocks of nature. All steriods and many other naturally occurring compounds are built from compound A. Spectroscopic analysis of A yields the following information:

IR : 3400cm-1;1640cm-1

H1NMR: 1.63δ (3H, singlet); 1.70δ (3H, singlet); 3.83δ (1H, broad singlet); 4.15δ (2H, doublet, J=7 Hz); 5.70δ (1H, triplet, J = 7 Hz)

  1. How many double bonds and/or rings does A have?
  2. From the IR spectrum, what is the identity of the oxygen-containing functional group?
  3. What kinds of protons are responsible for the NMR absorptions listed?
  4. Propose a structure for A.

Question: Give IUPAC names for the following compounds:

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