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Alcohol in which the hydroxyl is attached to a carbon attached to three other carbons?
Tertiary
How many isomers are there with molecular formula C7H14O and a five-membered ring and a tertiary alcohol group?
For the molecular formula C7H14O with a five-membered ring and a tertiary alcohol group, there are a limited number of isomers. A tertiary alcohol requires the hydroxyl (-OH) group to be attached to a carbon that is itself bonded to three other carbons. Given the constraints of forming a five-membered ring and maintaining a tertiary alcohol, there are 3 distinct isomers that fit these criteria.
Why does tertiary butyl alcohol and 2butanol mix with water?
They are polar compounds.
What classification of alcohol undergoes oxidation to yield a ketone?
A secondary alcohol undergoes oxidation to yield a ketone; a primary alcohol forms an aldehyde instead, and a tertiary alcohol usually does not form either a ketone or an alcohol, because the carbon having the OH group in a tertiary alcohol already has three bonds to other carbon atoms and therefore cannot form a double bond to oxygen without more extensive breaking of other bonds in the tertiary alcohol.
Compare the relative ease of oxidation of primary secondary and tertiary butyl alcohol toward acid dichromate based on the time required for the solution to change color?
primary alcohols react the fastest, with secondary alcohols next and tertiary alcoholsnot reacting at all. This is because the mechanism of this reaction is Sn1 which is a substituion reaction that favors attack on less crowded molecules
Is linalool an element?
No, linalool is not an element. It is a naturally occurring terpene alcohol found in many plants and is commonly used in the production of perfumes and flavorings.
Alcohol in which the hydroxyl is attached to a carbon attached to three other carbons?
Tertiary
How do you convert secondary alcohol to tertiary alcohol?
A secondary alcohol can be converted to a tertiary alcohol by subjecting it to an acid-catalyzed rearrangement reaction known as a pinacol rearrangement. In this process, the secondary alcohol undergoes a rearrangement to form a more stable tertiary alcohol through a carbocation intermediate.
Is a 2-methylpentan-3-ol a primary or secondary or tertiary alcohol?
it is a secondary alcohol
The single oxidation of a tertiary alcohol forms?
no reaction.
What is the relative reactivity of Secondary and tertiary alcohols towards oxidation with potassium permanganate?
Tertiary alcohols are more reactive towards oxidation with potassium permanganate compared to secondary alcohols. This is because the presence of more alkyl groups in tertiary alcohols stabilizes the intermediate carbocation formed during oxidation.
Why does tertiary butyl alcohol and 2butanol mix with water?
They are polar compounds.
What classification of alcohol undergoes oxidation to yield a ketone?
A secondary alcohol undergoes oxidation to yield a ketone; a primary alcohol forms an aldehyde instead, and a tertiary alcohol usually does not form either a ketone or an alcohol, because the carbon having the OH group in a tertiary alcohol already has three bonds to other carbon atoms and therefore cannot form a double bond to oxygen without more extensive breaking of other bonds in the tertiary alcohol.
Compare the relative ease of oxidation of primary secondary and tertiary butyl alcohol toward acid dichromate based on the time required for the solution to change color?
primary alcohols react the fastest, with secondary alcohols next and tertiary alcoholsnot reacting at all. This is because the mechanism of this reaction is Sn1 which is a substituion reaction that favors attack on less crowded molecules
What is the product when a tertiary alcohol is oxidized?
The product of oxidizing a tertiary alcohol is a ketone. Tertiary alcohols cannot be further oxidized to carboxylic acids due to the absence of a hydrogen atom on the carbon atom adjacent to the hydroxyl group.
What is the formula for tertiary alcohol?
molecular formula is C4H10O also written as (CH3)3COH
How acetone can be converted into tertiary butyl alcohol?
Acetone can be converted into tertiary butyl alcohol through a multistep process. First, acetone is converted to isopropanol using a reducing agent like sodium borohydride. Then, isopropanol is converted to diisopropyl ether using an acid catalyst like sulfuric acid. Finally, diisopropyl ether is converted to tertiary butyl alcohol through acid-catalyzed dehydration.
