Examples of 'secondary alcohols' in a sentence

Meaning of "secondary alcohols"

secondary alcohols: a type of alcohol compound where the carbon atom with the hydroxyl group is attached to two other carbon atoms
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  • plural of secondary alcohol

How to use "secondary alcohols" in a sentence

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secondary alcohols
Primary and secondary alcohols are easily oxidized.
A new method for the deoxygenation of secondary alcohols.
Only primary and secondary alcohols are oxidized.
Secondary alcohols are converted into ketones.
The equivalent secondary alcohols can also be used.
Process for production of ketones from secondary alcohols.
Guerbet or secondary alcohols or alkyl aromatic in nature.
More rarely used are secondary alcohols.
The secondary alcohols are preferably used.
Etherification of primary and secondary alcohols.
Secondary alcohols can be stereochemically inverted by formation of a formyl ester followed by saponification.
Both primary and secondary alcohols can be used.
Particularly suitable are primary or secondary alcohols.
The formation of secondary alcohols by the enantioselective addition of dialkylzincs to aldehydes is known.
Transglycosylation of primary and secondary alcohols.

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Secondary alcohols may require use of excess alcohol and longer reaction times.
Selective hydrolysis of cyclic secondary alcohols.
Production of ether from secondary alcohols such as isopropanol and light olefins is known.
Grignard reagents add to propylene oxide to give secondary alcohols.
Suitable functional groups include primary and secondary alcohols as well as dicarboxylic acids or anhydrides.
Hydrogen peroxide has been formed by the oxidation of secondary alcohols.
Acid chlorides react with primary and secondary alcohols to give esters in good yield.
In these methods primary alcohols are thiolated preferentially over secondary alcohols.
Mixtures of alcohols comprising primary and secondary alcohols are also suitable for use herein.
This material is an excellent transesterification catalyst for primary and secondary alcohols.
The system also enables a chemoselective oxidation of secondary alcohols in the presence of primary alcohols.
The esterification rate is slower with tertiary alcohols than primary or secondary alcohols.
Synthesis of such nitroimidazole secondary alcohols is presented in part B of this example.
Subsequent hydrogenation of the ketone wil result in secondary alcohols.
Additionally, secondary alcohols may also be present.
Selective reaction of primary alcohols in the presence of secondary alcohols is possible.
Analogously, secondary alcohols can be oxidized to form ketones.
Primary alcohols react slowly and secondary alcohols react rapidly.
The resulting catalyst was then used for the chemoselective oxidation of primary and secondary alcohols.
Aromatic ketones, secondary alcohols and related esters.
This is because primary alcohols generally react more rapidly than secondary alcohols.
Products would be primary alcohols, secondary alcohols or an amine, respectively.
Tertiary alcohols for instance are dehydrated with considerably greater ease than primary and secondary alcohols.
However, secondary alcohols have limited reactivity compared with primary alcohols.
An efficient reagent for oxidation of primary and secondary alcohols to carbonyl compounds.
Ketones give secondary alcohols while aldehydes, esters and carboxylic acids give primary alcohols.
Suitable functional groups include primary and secondary alcohols and carboxylic acids.
Primary or secondary alcohols containing 2 or 3 carbon atoms are preferably used.
Preferred solvents for cyclosporins include lower primary or secondary alcohols and propanone.
A number of primary and secondary alcohols was tested, from methanol to 2-butanol.
DCC can also be used to invert secondary alcohols.
Suitable paraffins for producing secondary alcohols are, for example, those produced from Fischer-Tropsch technologies.
Selective alkaline hydrolysis of the ester group of compounds V yielded the corresponding secondary alcohols VI.
In step a of the present process olefins, secondary alcohols or a mixture thereof are sulphated.
As an alternative, the branched alcohols may be branched secondary alcohols.

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