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.
Nucleophilic substitution reaction: nucleophilic substitution reaction is a reaction where the nucleophile attacks on the alkyl halide and replaces halogen atom during the reaction. Nucleophile substitution reactions are two types:
1.Uni-molecular nucleophilic reaction
2.Bi-molecular nucleophilic reaction
1.Uni-molecular nucleophilic reaction :
In this reaction, rate of the reaction depends only on substrate concentration, and carbocation is the intermediate in this reaction.
2.Bi-molecular nucleophilic reaction :
In this reaction, rate of the reaction depends on both substrate and reagent concentrations, and transition state is the intermediate in this reaction.
Ether reactivity with HI:
Ethers react with HI either in pathway; reaction mechanism of this reaction completely depends on the structure of the ether.
a.If the leaving group leaves first to form stable carbocation, this reaction follows .
b.If the leaving group leaves after associating with the nucleophile, this reaction follows .
The given reaction condition is drawn below.
The given substrate is ether and it is following .
The given reaction is drawn below with products during .
The above reaction follows , since ether gives the stable intermediate by leaving ethoxide ion.
Ans:The three products of the reaction are,
Benzyl ethyl ether reacts with concentrated aqueous HI to form two initial organic products (A and B). Further reacti...
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...
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.
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 both organic products of the following reaction. Hint:There will be two deuterium atoms in the benzyl alcohol product.
3. 1,2-dimethyl-1,3-cyclohexadiene reacts with HCl to form up to four different products. HCI 4 possible products a. b. Give the structures for the four products. When the reaction is run at low temperature, two products are formed preferentially ldentify these two products. c. When the reaction temperature is increased, a single product is favored. Identify the major product under these reaction conditions