Draw the structure(s) of the major organic product(s) of the following reaction.1. dioxane / 25°+CH32. aqueous acetic acid / reflux•You do not have to consider stereochemistry.• You do not have to explicitly draw H atoms.•Do not include lone pairs in your answer. They will not be considered in the grading.• Do not include the amine from which the enamine was derived.•If no reaction occurs, draw the organic starting material.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.?ChemDoodle<>

Answered: Image /qna-images/answer/afc12702-871e-475b-8430-fba12981dcab.jpg

Answered: Draw the structure(s) of the major…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter21: Nas: Nucleophilic Aromatic Substitution

Section: Chapter Questions

Problem 7E

See similar textbooks

Similar questions

Assume that 2-chloropropane reacts with CN− in an SN2 reaction. Use the JSME editor () to draw the structure of the substitution product of the reaction. The guide on how to draw your structure can be found here Important Note: When drawing the structures in the JME editor please adhere to the following formats: 1. If the nucleophile is OH−, DO NOT manually add the "H" to the final product 2. If the nucleophile is CN−, be sure to include the appropriate bonding between the C and N in the final product
What reaction would be best for preparing 2-isopropoxy pentane in high yield? 2-iodopentane and sodium isopropoxide sodium hydride added to 2-pentanol, then 2-iodopropane mercury acetate added to 1-pentene and isopropanol, then NaBH4 mercury acetate added to 2-pentene and isopropanol, then NaBH4
what is the purpose of adding concentrated sulfuric acid to a product after distillation? what products would you expect to be produced if H2SO4 were used as the acid catalyst, and an equimolar mixture of NaCl and NaBr were used as the sources of nucleophiles? Based on the previous question: more than one product is actually produced. Will the products be produced in equal amounts. why or why not
Reaction with Alcohols (esterification)a. Mix 1 mL of glacial acetic acid, 1 mL of ethyl alcohol and 3 drops ofconcentrated sulfuric acid (CAUTION!). Cautiously note the odor.Result: ___________________________________________________________________To what compound is the odor due? ________________________________________Equation: _________________________________________________________________b. To about 0.1 gm of salicylic acid in a test tube, add 1 mL of methyl alcoholand 3 drops of concentrated sulfuric acid (CAUTION!). Heat the mixture gentlyfor 1 – 2 minutes, then pour the mixture into about 20 mL of cold watercontained in a beaker. Observe the odor of the product formed. _____________What compound produces this odor? ______________________________________Equation: ______________________________________________________________
a. Can you predict an undesirable side reaction that might occur using ethanol as a solvent that would not occur if we used THF as a solvent?b. Based on your knowledge of SN2 reactions, what would happen if we used 1-ethyl-2- naphthoxide instead of 2-naphthoxide? Explain.
. A colorless liquid, C4H6O, having a boiling point of 97-98°C was found to be soluble in water and also in ether. It gave a negative test for the presence of halogens, sulfur, and nitrogen. It did however, give a positive test to 2,4-dinitrophenylhydrazine reagent. It gave a negative result when treated with ceric nitrate solution and also Tollen’s reagent. Treatment with ozone followed by hydrolysis in the presence of zinc gave formaldehyde as one of the products. What is the structure and name of the colorless liquid?
The addition of an alcohol to an acid chloride is an example of alcoholysis (alcohol addition with bond breakage). Consider the alcoholysis reaction below and answer the questions that follow. 1. Show the tetrahedral intermediate that is formed after the nucleophilic addition of the alcohol to the acid chloride. Be sure to include all lone pair electrons and formal charges on your intermediate structure. 2. Show the final product of this alcoholysis reaction that forms after the intermediate you made in Part 1. Do not include inorganic or charged products in your answer. Be sure to include all lone pair electrons and formal charges.
In the addition of just 1 mole of bromine to 1 mole of hex-1-yne, should the hex-1-yne be added to a bromine solution or should the bromine be added to the hex-1-yne? Explain your answer.
Write TRUE if the statement is correct and FALSE if the statement is wrong. Please answer them all Substitution reactions do not occur in aromatic rings because of pi-electron delocalization. The resulting iodinated aspirin has a higher Rf compared to aspirin after visualizing with ferric chloride. The mobile phase used in determining the Rf of the iodinated aspirin is 5% ethyl acetate in acetic acid. When isopropyl alcohol reacts with HCI, the resulting product is 2-chloropropane. In Fehling's test, the theoretical product after an aldehyde is mixed with Fehling's Solution is alcohol. lodoform, which has a molecular formula of CH3l, is indicative that a ketomethyl group is present. Based on the physical property, hydroquinone has a lower boiling point compared to catechol. Picric acid, being a phenolic compound, tests positive for the FeCl3 test. Nucleophilic molecules are electron-rich molecules that can "attack" electron-deficient molecules. When FeCl3 is used in visualizing…
How to use GC in this experiment to confirm the identity of product?
In the lab for the synthesis of methyl m-nitrobenzoate from methyl benzoate using HNO3 and H2SO4 via EAS, the product is recrystallized to remove impurities using 95% ethanol. Would o-nitrobenzoate and methyl p-nitrobenzoate be considered impurities? If that is so, how come ethanol can remove o-nitrobenzoate and methyl p-nitrobenzoate, but has no effect on m-nitrobenzoate? Thank you.
Please help me find the theoretical yield of these reactions. Reaction one is 0.50 grams of bromotriphenylmethane and 5.0 ml of ethanol. The second reaction is 1.5 mL of 1-bromopentane, 1.9 mL aniline and 3 mL of acetone.

SEE MORE QUESTIONS

Recommended textbooks for you

Organic Chemistry: A Guided Inquiry

Chemistry

ISBN:

9780618974122

Author:

Andrei Straumanis

Publisher:

Cengage Learning

Organic Chemistry

Chemistry

ISBN:

9781305580350

Author:

William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:

Cengage Learning

Organic Chemistry: A Guided Inquiry

Chemistry

ISBN:

9780618974122

Author:

Andrei Straumanis

Publisher:

Cengage Learning

Organic Chemistry

Chemistry

ISBN:

9781305580350

Author:

William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:

Cengage Learning

SEE MORE TEXTBOOKS