Alkenes on reacting with ozone results in the formation of ozonide which undergo reductive cleavage in presence of dimethyl sulfide to form carbonyl compounds (aldehyde or ketone). Whereas in presence of hydrogen peroxide it undergoes oxidative cleavage to form carboxylic acids or ketones.
Since, A alkene yields 4-heptanone only on treatment with ozone and DMS thus, it implies that both the chains on the side of the double-bond are similar the product is 4-heptanone that means the double bond is present between the chains at the 4th carbon. Therefore the structure of compound A is 4,5-dipropyloct-4-ene.
The reaction is as shown in the image.
The reaction of A with m-CPBA (meta-perchlorobenzoic acid) followed by aqueous acid 
is shown in the image.
m-CPBA (meta-perchlorobenzoic acid) is a peracid and forms epoxides on reacting with alkenes.
The question is incomplete, the complete question is shown in the image attached
Answer:
3-isopropyl-1-hexyne
Explanation:
Organic compounds can be named from the structure of the compound. The name reveals the arrangement of atoms and bonds in the molecule.
If we look at the compound in the question, we will notice that the parent chain contains six carbon atoms, the triple bond is located at position 1 and the isopropyl substituent is attached to carbon 3.
Hence the proper name of the compound becomes, 3-isopropyl-1-hexyne.
There are 7 trees that have to be harvested
Answer:
Explanation:
How do I describe an ion?
<h2>an ion is an atom that has had electrons added or taken away from it.</h2><h2>they do this in order to obtain a stable electronic configuration like their closest noble gas..see Periodic Table column 18 which is also column VIIIA</h2><h2>If they gain electrons, they are negative and are called</h2><h2>ANIONS</h2><h2>if they lose electrons they are positive and are called</h2><h2>CATIONS </h2><h2 />
