Question

When 5 -decyne is heated with diborane at \(160^{\circ}\) and the product is oxidized with hydrogen peroxide in basic solution, 1,10 -decanediol is obtained. Write equations to show the several reactions involved in these transformations. You need not show detailed mechanisms.

Short answer

5-decyne undergoes hydroboration and oxidation to yield 1,10-decanediol.

Step-by-step solution

React 5-decyne with Diborane

The first reaction involves the addition of diborane \((B_2H_6)\) to 5-decyne. This leads to the syn-addition of boron and hydrogen across the triple bond of 5-decyne, converting it into an alkene.

Perform Hydroboration

The product from Step 1, now an alkene, undergoes further hydroboration. This process involves the addition of two boron-hydrogen bonds across the alkene, leading to trialkylborane formation.

Oxidize with Hydrogen Peroxide

The trialkylborane is then reacted with hydrogen peroxide \((H_2O_2)\) in the presence of a basic solution, typically sodium hydroxide \((NaOH)\). This results in the oxidation of the intermediate to form the corresponding diol, which is 1,10-decanediol.

Key concepts

Hydroboration-Oxidation

The hydroboration-oxidation reaction is a two-step process used effectively for converting alkynes into alcohols. In this transformation, the central role is played by the reactivity and selectivity of boron compounds. In the first step, hydroboration, boron atoms are added across the carbon-carbon multiple bonds. This is usually achieved by using diborane \(B_2H_6\), which provides two boron-hydrogen groups that add syn-additionally across the alkyne bond.
This results in the formation of alkene intermediates.

• Hydroboration adds boron and hydrogen in a non-Markovnikov manner, attaching the boron to the less substituted carbon atom.
• The reaction converts a triple bond to a single bond by sequentially adding groups to either side of the bond.

These intermediates can then be oxidized to alcohols in the oxidation step. Here, hydrogen peroxide \(H_2O_2\) with a base like sodium hydroxide \(NaOH\) is used, converting the boronate to an alcohol. This is a clean reaction that often yields high purity alcohols after complete oxidation.

Alkyne Chemistry

Alkyne chemistry involves numerous reactions characterizing the triple-bond functional group. Alkynes are unsaturated hydrocarbons featuring a carbon-carbon triple bond. Their linear structure changes significantly upon hydrogenation or other addition reactions.

• Alkynes' triple bonds make them more reactive compared to alkenes and alkanes due to the high energy and accessibility of their electrons.
• They undergo addition reactions that fully saturate the triple bond, thereby converting it into an alkene and further to an alkane if fully hydrogenated.
• The process of adding elements can be controlled to halt at the alkene stage, particularly using the hydroboration method described above.

In the exercise, 5-decyne starts as an alkyne, and through careful hydroboration-oxidation, it's transformed first to an alkene, then fully converted to a diol—showing how alkyne chemistry can be skillfully exploited to tailor desired products.

Diol Formation

Diol formation refers to the process where two hydroxyl groups are added, typically across what originally was a double or triple bond, forming vicinal diols, or those with hydroxyl groups on adjacent carbons. In the exercise, 5-decyne ultimately transforms through several reactions into 1,10-decanediol—a molecule with hydroxyl groups on the first and tenth carbon atoms.

• The transformation begins with the hydroboration of 5-decyne, which forms an alkene with boron groups.
• Subsequent oxidation replaces the boron with hydroxyl groups, resulting in a stable, non-reactive 1,10-decanediol.
• The choice of reagents like diborane and the oxidizing agent \(H_2O_2\) ensures that the diol formation is controlled and yields the precise product.

This process is particularly valuable in organic synthesis to create specific diols that can serve as building blocks for more complex molecules, demonstrating another level of versatility and precision in synthetic chemistry.