44 > Draw the structures of the carboxylic acid and the alcohol that produce the ester shown in an esterification reaction. Include all hydrogen atoms in the structures. carboxylic acid Select Draw Templates More / # C O H CH3 H3C-C H alcohol Submit Answ HCI CH 3 -C-O-CH2-CH3 Erase Select Draw Templates More / # # C 0 H B Q Search Erase

44 > Draw the structures of the carboxylic acid and the alcohol that produce the ester shown in an esterification reaction. Include all hydrogen atoms in the structures. carboxylic acid Select Draw Templates More / # C O H CH3 H3C-C H alcohol Submit Answ HCI CH 3 -C-O-CH2-CH3 Erase Select Draw Templates More / # # C 0 H B Q Search Erase

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter17: Alcohols And Phenols

Section17.SE: Something Extra

Problem 37AP: Give IUPAC names for the following compounds:

See similar textbooks

Similar questions

Wanswered add hydrolysis 1 What products are formed in the acid hydrolysis of the compound shown below? CH3 C--0-CH, CH3 Salect an answerand submit. For keyboard'navigation, Lse the up/down arrow keys to select an answer. Aceticacid and water Propanoic acid and ethanol ic. Ethanol and acetic acid Ethanaland ethand Acrriciane anicthang
Draw the structure of the organic product that is formed when the compound shown below is treated with the following reagents: 1) TsCl, pyridine; 2) NaCN. Interactive 3D display mode H₂Cl OH Draw the molecule on the canyas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single be
1. NaOEt CO₂Et 2. H3O+ 3. heat Br H3C H₁C CO₂Et CO₂H CO2 + EtOH The malonic ester synthesis is a carbonyl alkylation reaction. It is used to prepare carboxylic acids from primary alkyl halides, lengthening the carbon chain by two atoms. Thus, the product can be visualized as being a "substituted acetic acid." The reaction consists of three steps: generation of the enolate anion followed by SN2 reaction with a primary alkyl halide, ester hydrolysis under acid conditions, and decarboxylation. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions EtO₂C X ¯:0: :0: Br: EtO₂C. Br CH3 H3C CH3 CH3 56
15
Claisen condensation between diethyl phthalate and ethyl acetate followed by saponifi- cation, acidification, and decarboxylation forms a diketone, C,H,O,. COOEt 1. EtO Na+ HCI, H,O B NaOH, H,O + CH3COOEt C,H,O2 2. НС, Н,О heat heat COOEt Diethyl phthalate Ethyl acetate Propose structural formulas for compounds A and B and the diketone.
Draw the organic product formed in the reaction.
possible products of the reaction below
Give IUPAC names for the following compounds:
13:22 4G O 5 ê © T Ô 1. What is the correct IUPAC name for the following compound? Q A. Diphenylamine 1,1 diphenylamine OCN,N-diphenylamine O D. None of the above is correct Add a caption... > Status (Custom) +
1. NaOEt CO₂Et 2. H3O+ 3. heat Br H3C CO₂H CO2 H3C CO₂Et The malonic ester synthesis is a carbonyl alkylation reaction. It is used to prepare carboxylic acids from primary alkyl halides, lengthening the carbon chain by two atoms. Thus, the product can be visualized as being a "substituted acetic acid." The reaction consists of three steps: generation of the enolate anion followed by SN2 reaction with a primary alkyl halide, ester hydrolysis under acid conditions, and decarboxylation. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions 22 CX EtO₂C EtO₂C HOCH2CH3 HOCH2CH3 EtO₂C EtO₂C
27) Hydrolysis of an ester: O II CH,-C-O-CH2-CH2-CH, + H20 28) Acid/ Base reaction of an amine CH3-CH2-NH2 H2CO3 29) Hydrolysis of an amide 11 CH3-CH2-CH2-CH2-CH2-C-NH-CH2-CH2-CH, + H20 OMIC Molecules
For the following lise ONLY reactions we have studied in cla Powerpoint slides for preparations and reactie you Check your APPS out 6 contpletely different reactions of acetophenone trea b) Write out 3 preparations of 2-methyl-2-butanol, using a different starting material for each one. You may use preps where you just change the functional group, and/or preps where you construct the carbon chain. group ind/o Juc