Diisopropyl ether reacts with concentrated aqueous HI to form two initial organic products
1 answer:
Answer:
True
Explanation:
The reaction between Diisopropyl ether and concentrated aqueous HI forms two initial organic products as shown in the image attached.
The hydrogen of the HI becomes attached to the oxygen in the ether leading to a cleavage of the C-O bond to yield the first compound. The I^- become attached to the other moiety in the original molecule to yield the second compound as shown in the image attached.
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Answer:
It has been drawn and uploaded as an attachment. Please download it to see the structure.
Explanation:
The product formed as a result of the reaction of cyclohexene with H2 in presence of Pt (platinum) can be described as catalytic hydrogenation. Catalytic hydrogenation is defined as the process of hydrogen addition in the presence of a catalyst, which in this case is platinum.
Note that Cyclohexene (alkene) is a hydrocarbon molecule represented by the chemical formula, C6H10 .
It consists of a double bond. During the hydrogenation reaction, the alkene undergoes an addition reaction to give alkane which is a saturated hydrocarbon as the product.
The first step in order to derive the product is to draw the chemical structure of cyclohexene and identify the double bond present in it.
The final product can be derived by replacing the double bond with the single bond and satisfying all the valences of the carbon atom. The final product structure has been drawn and uploaded as an attachment. Please download it to see the structure.
Ans:
The structure of the cyclohexane thus, formed has been shown as follows with all the hydrogen atoms:
