The concept used to solve the first question is cleavage of ether takes place with strong acid, HI and forms an alcohol, alkyl iodide, which is further reacted with HI to form second alkyl iodide.
The mechanism of ether cleavage takes place via or .
With the methyl or primary alkyl groups that are bonded to ether oxygen, the cleavage of C-O bond takes place via mechanism. Similarly, with the secondary or tertiary alkyl groups that are bonded to ether oxygen, the cleavage of C-O bond takes place via mechanism.
The reaction is as follows:
The reaction is as follows:
Ans:The structures of three products are as follows:
Benzyl ethyl ether reacts with concentrated aqueous HI to form two initial organic products (A and B). Further reaction...
Benzyl ethyl ether reacts with concentrated aqueous HI to form two initial organic products (A and B). Further reaction of product B with HI produces organic product C. Draw the structures of these three products.
Diisopropyl ether reacts with concentrated aqueous HI to form two initial organic products (A and B). Further reaction with HI produces organic product C from product B. Draw the structures of these three products.
Diisopropyl ether reacts with concentrated aqueous HI to form two initial organic products (A and B). Further reaction with HI produces organic product C from product B. Draw the structures of these three products.
2-Ethoxy-2,3-dimethylbutane reacts with concentrated aqueous HI to form two initial organic products (A and B). Further reaction with HI produces organic product C from product B. Draw the structures of these three products.
2-Ethoxy-2,3-dimethylbutane reacts with concentrated aqueous HI to form two initial organic products (A and B). Further reaction with HI produces organic product C from product B. Draw the structures of these three products.
Ethers react with HI to form two cleavage products. One of the products might react further with HI. In the first box below draw the two major products that could be recovered after treatment with one equivalent of HI. In the second box draw the two major products that could be recovered after treatment with excess HI. (If a product of the first step does not undergo additional reaction with excess HI, repeat its structure in the second box.) Ethers...
The term "side reactions" refers to any chemical reaction that can occur that form products other than the desired product. Side reactions can consume the reactants of your intended reaction, and can affect the percent yield of your target product. One possible side reaction produces butyl ethyl ether. Draw the complete reaction mechanism for the formation of butyl ethyl ether as a side product 2 Marks]
Draw the most stable form of the organic products formed in the following reacton of ethyl acetate and ethyl benzoate. Ethanol can be excluded from your answer. The product already there is correct and is the mixed Claisen condensation product. I also need the unmixed Claisen product.
Draw both organic products of the following reaction. Hint:There will be two deuterium atoms in the benzyl alcohol product.
Draw the final products for the following two step reaction. The nucleophile selectively reacts once in each step. Draw the major organic product(s) produced in the following reaction. Draw all possible products produced in the following reaction. Draw the starting materials (electrophile as an alkyl bromide) needed to complete the following reaction. The mechanism for this reaction follows a SN1 pathway.