**Question 16 of 27****Problem Statement:**"Draw the major product of this aminolysis reaction. Ignore inorganic byproducts."**Chemical Structure and Reaction Details:**- **Reactant:** The structure shown is a linear dicarbonyl compound with two ester groups. - **Reagent:** `excess NH(CH₃)₂` (dimethylamine)**Diagram Description:**- Two carbonyl groups are connected via ester linkages in the reactant.- An arrow pointing downward indicates the addition of dimethylamine in excess.- Below the arrow, there is a dashed box labeled "Select to Draw."**Instructions:**You are required to draw the major organic product formed by the reaction of the given ester with excess dimethylamine. The aminolysis will likely replace the ester group with an amide. Focus on the transformation of functional groups and ensure to consider the impact of excess amine in the reaction pathway. Ignore any inorganic byproducts in your drawing.

Answered: Image /qna-images/answer/024387e7-c1b5-46d3-a786-954bad46b2a9.jpg

Answered: Draw the major product of this…

Science

Chemistry

Draw the major product of this aminolysis reaction. Ignore inorganic byproducts.

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Similar questions

Draw the major product of this aminolysis reaction. Ignore inorganic byproducts. excess NHз Q
Identify the part of a generic amino acid that reacts with base and the part that reacts with acid. Briefly explain your answer.Hint: Draw Lewis structures for ammonia (NH 3) and acetic acid (CH 3COOH).
This amino acid would be more likely to bind to a receptor inside of the cell. COO- H3N-C-H CH2 CH2 CH2 CH2 *NH3 True O False This amino acid would be more likely to bind to a receptor inside of the cell. COO H3N-C-H H-C-CH3 CH2 CH3 O True O False
Which statement is NOT true about a peptide bond? O The peptide bond is longer than the typical carbon-nitrogen bond. CO The carbonyl oxygen and the amide hydrogen are most often in a frans configuration with respect to another. O Rotation is restricted about the peptide bond. The peptide bond has partial double-bond character.
What are the structures of the amino acids that result from the hydrolysis of all the peptide bonds in the peptide? HO 'N' HO, NH2 H COOH draw structure ... draw structure ... draw structure .. left structure middle structure right structure
Two of the amino acids have two chiral centers. Give the name and three-letter abbreviation of each. Enter your answers separated by a comma.Enter your answers separated by a comma.
Select the methods of synthesis that could be used to make the following amino acid. These reactions are presented in section 21.6 of your text. I have provided them in abbreviated generic form below in case you might find this helpful. Note that I have edited the Strecker synthesis to allow for the possibility of a ketone instead of an aldehyde as the starting material. (The text shows only aldehydes as reactants.) H,N, OH CH, 1) Br,, PBr3 Hell-Volhard-Zelinski R R. 2) H,O 3) excess NH3 `OH OH NH, 1) excess NH3 Reductive amination ОН НО. 2) H2, Pd/C NH, R' 1) NH3 R Strecker HO, 2) HCN R `R' 3) HCІ, Н,0, д NH, 1) potassium phthalimide R' Phthalimidomalonic ester RO OR 2) RO© НО. Br 3) R'-Br NH, 4) НCІ, H,0, Д O Hell-Volhard-Zelinski (HVZ) O Reductive amination O Strecker O Phthalimidomalonic ester
NEED HELP ASAP