Examples of 'tertiary alcohols' in a sentence
Meaning of "tertiary alcohols"
tertiary alcohols - Tertiary alcohols are a type of alcohol compound in organic chemistry characterized by a hydroxyl (-OH) group attached to a carbon atom that is bonded to three other carbon atoms. They have distinct chemical properties and are commonly found in various organic molecules
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- plural of tertiary alcohol
How to use "tertiary alcohols" in a sentence
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tertiary alcohols
Ethers are not formed by secondary or tertiary alcohols.
Tertiary alcohols are prone to elimination.
Treatment with ketones leads to tertiary alcohols in high yield.
Tertiary alcohols are more reactive than secondary or primary alcohols.
This method is particularly well suited to derivatization of tertiary alcohols.
Tertiary alcohols are thus mainly obtained from branched alkanes.
Grignard reagents react with carbonyl groups to secondary and tertiary alcohols.
Cyclic tertiary alcohols and their use as perfuming ingredients.
The esterification rate is slower with tertiary alcohols than primary or secondary alcohols.
Tertiary alcohols are resistant to oxidation.
The present invention relates to an improvement in the preparation of secondary and tertiary alcohols.
And the chromates of tertiary alcohols remain useful as oxidizing agents.
Can be treated with a variety of nucleophiles to form tertiary alcohols of structure XIX.
The tertiary alcohols derived from this reaction are then subjected to a dehydration.
These methods are illustrative of how secondary grid tertiary alcohols are made to these series.
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Secondary and tertiary alcohols react with hydrogen chloride to give the corresponding chlorides.
These again can be subjected to a Grignard reaction to obtain the tertiary alcohols described herein.
Tertiary alcohols can be derivatized with higher yields and improved purity via this method.
Then by hydrolysis, tertiary alcohols can be synthesized.
Tertiary alcohols for instance are dehydrated with considerably greater ease than primary and secondary alcohols.
It is preferred to use primary, secondary or tertiary alcohols.
Thus secondary and tertiary alcohols are acceptable solvents but primary alcohols can displace fluoride.
However, this list excludes all tertiary alcohols.
Only secondary and tertiary alcohols undergo the Riemschneider reaction.
The alcohols may be primary, secondary or tertiary alcohols.
Esters can be converted to tertiary alcohols with a Grignard reagent or an alkyl lithium reagents.
Suitable solvents are primary, secondary and tertiary alcohols.
Preferably, the tertiary alcohols are monohydric alcohols.
Examples of suitable alcohols include primary, secondary or tertiary alcohols.
Halo-biphenyl tertiary alcohols useful in therapy in the treatment of atherosclerosis.
Explain primary, secondary and tertiary alcohols with examples.
Magic acid catalyzes cleavage-rearrangement reactions of tertiary hydroperoxides and tertiary alcohols.
Primary, secondary and tertiary alcohols were used for this study.
Preferably, the solvent does not comprise any secondary or tertiary alcohols.
Although secondary or tertiary alcohols may be used, primary alcohols are preferred.
The ethers may derive from primary, secondary or tertiary alcohols.
However, such simple tertiary alcohols are rarely degraded by bacteria or other microorganisms.
Such biuretizing agents include water, secondary monoamines and tertiary alcohols.
Tertiary alcohols eliminate easily at just above room temperature, but primary alcohols require a higher temperature.
Lucas test is used to distinguish between primary, secondary, and tertiary alcohols.
Secondary and tertiary alcohols dehydrate through the E1 mechanism.
Lucas test in alcohols is a test to differentiate between primary, secondary, and tertiary alcohols.
Tertiary alcohols are unreactive towards peroxy hygiene agents such as ( a ).
The alcoholic medium can consist of one or more primary, secondary or tertiary alcohols.
Preferred tertiary alcohols are tert-butanol and ter-amyl alcohol.
Organo-tin catalysts have been used to prepare a large number of new carbamates of tertiary alcohols.
Among these, secondary and tertiary alcohols such as 2-propanol and tert-butanol are preferred.
Consequently, a special technology with the use of substrate-specificity is employed to obtain tertiary alcohols.
For the tertiary alcohols the general form is RR'R " COH.
In addition . the cyclic pro-perfumes described herein are capable of delivering highly desirable tertiary alcohols.
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