Nitriles Sentence Examples

When distilled with phosphoric anhydride they yield nitriles.

The same difference attends the introduction of the methyl group into many classes of compounds, for example, the paraffins, olefines, acetylenes, aromatic hydrocarbons, alcohols, aldehydes, ketones and esters, while a slightly lower value (157.1) is found in the case of the halogen compounds, nitriles, amines, acids, ethers, sulphides and nitro compounds.

The combination of nitrogen with carbon may result in the formation of nitriles, cyanides, or primary, secondary or tertiary amines.

The syn-aldoximes or treatment with acetyl chloride readily lose water and yield nitriles; the anti-aldoximes as a rule are acetylated and do not yield nitriles.

An important nucleus-synthetic reaction is the saponification of nitriles, which may be obtained by the interaction of potassium cyanide with a halogen substitution derivative or a sulphonic acid.

They may be prepared by converting nitriles into amidoximes by the action of hydroxylamine, the amidoximes so formed being then acylated by acid chlorides or anhydrides.

It combines with aldehydes and ketones to form the nitriles of oxy-acids, for example, CH 3 CHO+HCN=CH 3 CH(OH)(CN).

Its nitrile (prussic acid) has an acid character, a property not possessed by the nitriles of the other members of the series; and, by the abstraction of the elements of water from the acid,.

In the case of iodine, the substitution is effected by adding a warm solution of potassium iodide to the diazonium solution, no copper or cuprous salt being necessary; whilst for the production of nitriles a solution of potassium cuprous cyanide is used.

Bernthsen); by the action of ammonium chloride or hydrochlorides of amines on nitriles; by condensing amines and amides in presence of phosphorus trichloride; by the action of hydrochloric acid on acid-amides (0.

On dry distillation they yield nitriles and ammonia.

It also acts in an opposite manner in certain cases, adding the elements of water to compounds; thus, nitriles are converted into acid-amides, and various acetylene derivatives may be caused to yield ketonic derivatives.

However, NaBH 4 isn't a strong enough reducing agent to reduce nitriles.

Indeed, the role of simple nitriles as cycloaddition reagents has only been reported this year [22] .