There is no acid formation produced when primary alcohols are used.

Primary alcohols do not react appreciably with Lucas reagent at room temperature.

A minor pathway is oxidation of the terminal methyl groups to primary alcohols.

Primary alcohols will be oxidised to aldehydes and not carboxylic acids.

Examples of primary alcohols include ethanol and butanol.

Primary alcohols do not work well.

HI is also used in organic chemistry to convert primary alcohols into alkyl halides.

Primary alcohols can be synthesized from aldehydes by hydrogenation.

The direct oxidation of primary alcohols to carboxylic acids can be carried out using:

Primary alcohols can be protected in less than one hour while some hindered alcohols may require days of reaction time.

However, PLD activity can be measured by the addition of primary alcohols to the cell.

Anti-ulcer activity of higher primary alcohols of beeswax.

Conversion of primary alcohols to carbamates.

This colorless pyrophoric liquid is mainly used to make linear primary alcohols and α-olefins.

Homologated primary alcohols result from the treatment of organoboranes with carbon monoxide and a hydride.

However, no oxidation to carboxylic acids occurs on allylic and benzylic primary alcohols.

Primary alcohols oxidise to form alkanones (keytones).

It is used to selectively oxidize primary alcohols to the aldehyde, and will tolerate many other functional groups within the molecule.

Especially for fine chemical syntheses, lithium aluminium hydride is used to reduce esters to two primary alcohols.

The reagent is mostly used to convert primary alcohols to alkyl fluorides under mild conditions with high yield.

The oxide catalyzes dehydration of acyclic primary alcohols to aldehydes and ketones.

Benzilic acid is a white crystalline aromatic acid soluble in many primary alcohols.

It converts primary alcohols into aldehydes, or into carboxylic acids if heated under reflux.

Tertiary alcohols eliminate easily at just above room temperature, but primary alcohols require a higher temperature.

The oxidation of primary alcohols to carboxylic acids is an important oxidation reaction in organic chemistry.

The primary alcohol in wine and most other alcoholic beverages.

There is no acid formation produced when primary alcohols are used.

More specifically, it features three primary alcohol groups in a compact neopentyl structure.

It contains both a primary amine and a primary alcohol.

Tequila is the primary alcohol ingredient in a margarita.

Primary alcohol 2.1 was protected in preparation for lactone reduction in 2.3.

Primary alcohols do not react appreciably with Lucas reagent at room temperature.

A minor pathway is oxidation of the terminal methyl groups to primary alcohols.

Primary alcohols will be oxidised to aldehydes and not carboxylic acids.

Examples of primary alcohols include ethanol and butanol.

Primary alcohols do not work well.

By the mid-1990s, the town lost its status as the primary alcohol stop in the county as other nearby communities began to repeal their Blue laws.

Only primary alcohol oxidation is observed.

HI is also used in organic chemistry to convert primary alcohols into alkyl halides.

Primary alcohols can be synthesized from aldehydes by hydrogenation.

The direct oxidation of primary alcohols to carboxylic acids can be carried out using:

Primary alcohols can be protected in less than one hour while some hindered alcohols may require days of reaction time.

However, PLD activity can be measured by the addition of primary alcohols to the cell.

Anti-ulcer activity of higher primary alcohols of beeswax.

Conversion of primary alcohols to carbamates.

This colorless pyrophoric liquid is mainly used to make linear primary alcohols and α-olefins.

Homologated primary alcohols result from the treatment of organoboranes with carbon monoxide and a hydride.

The only primary alcohol and aldehyde to undergo this reaction are ethanol and ethanal, respectively.

When a primary alcohol is converted to a carboxylic acid, the terminal carbon atom increases its oxidation state by four.

A primary alcohol is an alcohol which has the hydroxyl group connected to a primary carbon atom.