You asked: Which of the following reagents converts alkene into alcohol?

With oxymercuration-demercuration, you have a reaction that converts alkenes into Markovnikov-product alcohols. To make the alcohol on the least-substituted carbon (called the anti-Markovnikov product) you use hydroboration, as shown in the next figure.

How do you convert alkenes to alcohol?

Alkenes can be converted to alcohols by the net addition of water across the double bond.

How are alcohols formed from alkanes?

The now negatively-charged strong acid picks up the green electrophilic hydrogen. Now that the reaction is complete, the non-nucleophilic strong acid is regenerated as a catalyst and an alcohol forms on the most substituted carbon of the current alkane. At lower temperatures, more alcohol product can be formed.

What is a secondary alcohol structure?

A secondary alcohol is a compound in which a hydroxy group, ‒OH, is attached to a saturated carbon atom which has two other carbon atoms attached to it.

Which alcohol is least soluble in water?

According to this, 1−pentanol will be the least soluble in water, among the other given alcohols.

Is 1 butanol an alcohol or alkane?

Explanation: The -ol suffix tells us that butanol is an alcohol. Butane is a 4 carbon alkane, but unlike butane, butanol has one of its hydrogens replaced with a hydroxyl group (-OH).

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Can alkynes be oxidised?

Alkynes, similar to alkenes, can be oxidized gently or strongly depending on the reaction environment. Since alkynes are less stable than alkenens, the reactions conditions can be gentler. For examples, alkynes form vicinal dicarbonyls in neutral permanganate solution.

Can alcohols be reduced to alkanes?

Reduction of Alcohols Normally an alcohol cannot be directly reduced to an alkane in one step. The –OH group is a poor leaving group so hydride displacement is not a good option – however the hydroxyl group is easily converted into other groups that are superior leaving groups, and allow reactions to proceed.

Which of the following is an example of a secondary alcohol?

In the case of a secondary alcohol, two carbon atoms are bonded to the alpha-carbon. Example – 2 – propanol and 2 – butanol.

Which of the following is a secondary allylic alcohol?

But-3-en-2-ol is a secondary allylic alcohol.

Secondary allylic alcohols are the allylic alcohols in which the carbon atom is linked with the double bond as well as to another carbon and also one hydrogen.

What are the examples of secondary alcohol?

An example of a secondary alcohol is:

  • A. 1-propanol.
  • B. 2-propanol.
  • C. 1,2-propanol.
  • D. 1,2,3- propanol.

Which alcohol is maximum soluble in water?

Hence, glycerol has the highest solubility in water and so the correct option is D.

Which alcohol is more soluble in water?

Ethyl alcohol is more soluble in water than dimethyl class 12 chemistry CBSE.

Which alcohol is most soluble in water?

Because of the strength of the attraction of the OH group, first three alcohols (methanol, ethanol and propanol) are completely miscible. They dissolve in water in any amount.

Alcohol solubility chart.

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Name Formula Solubility
Methanol CH3OH miscible
Ethanol C2H5OH miscible
Propanol C3H7OH miscible
Butanol C4H9OH 0.11
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