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.
The concept is to draw the three major organic products, when an ether (2-isopropoxypropane) reacts with concentrated HI.
Ethers react with strong acids such as HCl, HBr, and HCl they form alkyl halide and alcohols as products.
The reaction is,
The reaction is,
Ans:Thus, the structure of three product are,
Diisopropyl ether reacts with concentrated aqueous HI to form two initial organic products (A and B). Further reactio...
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.
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.
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.
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...
[Review Topical [References) 1-Butene reacts with borane in THF followed by hydrogen peroxide in aqueous NaOH to give A (CH100). Treatment of A with aqueous chromic acid or Cro, in acetic acid gives B (C,H,O,). Draw the structure of B. • You do not have to consider stereochemistry. . In cases where there is more than one answer, just draw one. ChemDoodle [Review Topics) [References) A (CzH,0) reacts rapidly with ethylmagnesium bromide in anhydrous ether to give B (C,H,20). Treatment...
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
Draw the structure(s) of the major organic product(s) of the following reaction Dilute aqueous HCI • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • If the reaction produces a racemic mixture, draw both stereoisomers. • Include counter-ions, e.g., Na, 1', in your submission, but draw them in their own separate sketcher. Omit products derived from the acidic or basic reagent itself, e.g. HN(i- Pr), derived from N(i-Pr)2 - • If substantial starting material is present at...
Acid-catalyzed dehydration of secondary and tertiary alcohols proceeds through an E1 mechanism. The first step is the protonation of alcohol and oxygen to form anoxonium ion.Dehydration of 3-methyl-2-butanol forms one major and two minor organic products. Draw the structures, including hydrogen atoms, of the three organic products ofthis reaction.The 3.) is correct that is the minor product I came up with but I cant get the answer correct for 1.) major product? and 2.) minor product