What happens when alkenes are oxidized?
Alkenes are oxidised to give carbonyl compounds or carboxylic acids depending upon the condition.
So ozonolysis is an example of oxidative cleavage reaction that leads to the breaking
- Oxidative ozonolysis
- Reductive ozonolysis
Let me begin with oxidative ozonolysis. In this reaction,
Now taking the second condition, i.e reductive ozonolysis.
In this case, oxygen is oxidized to intermediate form i.e carbonyl compound. The reductive workup is done with
Hope it helps!!
By signing up, you agree to our Terms of Service and Privacy Policy
When alkenes are oxidized, they undergo addition reactions with oxygen. This typically involves the formation of an epoxide or diol. The most common method of alkene oxidation is with potassium permanganate (KMnO4) or osmium tetroxide (OsO4), which adds two oxygen atoms across the double bond to form a diol. In some cases, the alkene may be cleaved to form carbonyl compounds such as aldehydes or ketones. The specific product formed depends on the reaction conditions and the structure of the alkene.
By signing up, you agree to our Terms of Service and Privacy Policy
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
- What product will we get from the reaction (i) C6H5CHO + CH3CH2OH (reagent HCl)→ (ii) CH3CH2C(Cl)2CHO + H20 (reagent H+) → ?
- Write the overall reaction for reaction of methyl benzoate with excess phenyl magnesium brimide in ether, followed by H3O+. ????
- Describe two chemical tests that can be used to distinguish between the following pair of compounds?
- What happens when alkenes are oxidized?
- Write the equation for the preparation of a Grignard reagent using 2-bromo-3-methylbutane and name the alkane produced after its hydrolysis?

- 98% accuracy study help
- Covers math, physics, chemistry, biology, and more
- Step-by-step, in-depth guides
- Readily available 24/7