Draw the major monoalkylation product(s) you would expect to obtain from reaction of p-chloroaniline with chloromethane and AlCl3. • You do not have to consider stereochemistry. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple products using the + sign from the drop-down menu. • If no reaction occurs, draw the organic starting material. opy aste opy aste CI Нас H,N, Н.N, Cl Cl ChemDoodle ChemDoodle An error has been detected in your answer. Check for typos, miscalculations etc. before submitting your answer. Submit Answer Try Another Version 8 item attempts remaining

Draw the major monoalkylation product(s) you would expect to obtain from reaction of p-chloroaniline with chloromethane and AlCl3. • You do not have to consider stereochemistry. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple products using the + sign from the drop-down menu. • If no reaction occurs, draw the organic starting material. opy aste opy aste CI Нас H,N, Н.N, Cl Cl ChemDoodle ChemDoodle An error has been detected in your answer. Check for typos, miscalculations etc. before submitting your answer. Submit Answer Try Another Version 8 item attempts remaining

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter13: Substitution

Section: Chapter Questions

Problem 2E

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Similar questions

Draw the organic product(s) of the following reaction. You do not have to consider stereochemistry. Include cationic counter-ions, e.g., Na+ in your answer, but draw them in their own sketcher. If no reaction occurs, draw the organic starting material. Separate multiple products using the + sign from the drop-down menu.
Write structures for the carbonyl electrophile and enolate nucleophile that react to give the aldol below. You do not have to consider stereochemistry. Draw the enolate nucleophile in its carbanion form. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple reactants using the + sign from the drop-down menu.
1-bromo-1-methylcyclopentane is being reacted with sodium ethoxide in diethyl ether Ethoxide will remove a proton from one of the carbons alpha to the carbon bonded to bromine. The electron pair from the carbon-hydrogen bond will move toward the 1 carbon to form a new pi bond. This will push off the bromine, which will leave with its electron pair to form a bromide leaving group. This will form the product 1-methylcyclopentene and sodium bromide as byproduct. So, is this reaction following an E1 or E2 mechanism? Write out the rate law for this reaction. Draw a reaction coordinate diagram for this reaction.
Draw the structure(s) of the major organic product(s) obtained after workup of the following reaction. Use the wedge/hash bond tools to indicate stereochemistry where it exists. If no reaction occurs, draw the organic starting material. Draw structure(s) of product(s) after aqueous workup. Include counter-ions, e.g., Na+, I-, in your submission, but draw them in their own separate sketcher. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner.
This question has multiple parts. Work all the parts to get the most points. a Draw all of the monochlorination products that you might obtain from the free-radical chlorination of 2,2-dimethylbutane. You do not have to consider stereochemistry. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple products using the + sign from the drop-down menu.
Why is the mechanism shown in Figure 28 not plausible? * A- The reagent does not have a good leaving group. B- Water is too weak a base for the reaction to occur. C- The structure of the haloalkane prevents the nucleophile from coming close to the alpha carbon atom. D- None of these statements are correct. E- All these statements are correct.
The compound shown below is the product of a Claisen condensation. Draw structural formulas for the reactants: ester and enolate ion. Assume all esters to be ethyl esters. Do not include counter-ions, e.g., Na+, I-, in your answer. Draw the enolate ion in its carbanion form. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple reactants using the + sign from the drop-down menu.
Draw the structure of the intermediate that forms in the first step of the reaction mechanism and the product. The electrophilic addition reaction in question 3, proceeds through two intermediates and three discrete mechanism steps. Using curved arrow formalism, draw the reaction mechanism for the transformation in question 3 with Br2 and H2O.
C6H5CO2CH2C6H5 can be synthesized by an SN2 reaction. Draw the structures of the alkyl chloride and nucleophile that will give this compound in highest yield. Use the wedge/hash bond tools to indicate stereochemistry where it exists. Include all valence lone pairs in your answer. Separate multiple reactants using the + sign from the drop-down menu. When a metal counterion is needed, use Na+, but draw it in its own sketcher.
Tertiary alcohols do not react to produce an ester, like we would expect in this experiment. Instead, a different product is formed. When t-butyl alochol (2-methyl-2-propanol) is used in this experiment, give the main organic product that would be formed.
a. Write the complete mechanism, step by step, for the reaction shown in the image A, in such a way that it explains the formation of the products (Please do not forget the correct use of arrows!). b. Write the complete mechanism (suppose an E2), step by step of the reaction shown in the figure B, in such a way that it explains the formation of a single product (DO NOT FORGET THE CORRECT USE OF THE ARROWS!). Using structures, justify the formation of the chosen product and not others. c. Write the complete mechanism (suppose a bimolecular reaction), step by step of the reaction shown in the figure C, in such a way that it explains the formation of all possible products (there are three). (DON'T FORGET TO USE THE ARROWS CORRECTLY!). Watch out for stereochemistry!
Monensin (1) is a potent antibiotic. JACS 1980, 102, 2118-2120. 1. Use arrows provided a pathway from (1) to (2) when we add a mild base sodium bicarbonate followed by iodine (I2). 2. What was a similar reaction between Br2 and an alkene? What did we name the intermediate?