ONANO(a) Circle the two compounds that are not carboxylic acid derivatives. Circle only two.CONHCH3CN=NOHNHCOCI(b) Circle the two compounds that can be hydrolyzed to a ketone in aqueous acid. Circle only two.N-PH(c) Circle the two compounds that can be converted to an aldehyde by reduction using DIBAL (also known asDIBAL-H). Circle only two..CHOонCN(d) Circle the two most reactive compounds with water. Circle only twoDEtOMeNH2CH;CH,CN(e) Circle the strongest acid. [2 marks]CO.EtCO-HNO2CHO(1) Circle ethyl benzoate and maleic anhydride.COCH,CH,.Co.CH,CH3(g) Circle the two compounds that can be reduced to an amine using NaBH4. Circle only two.'NH2CNNH

A. Carboxylic acid derivatives are : ester, amide, nitrile, anhydride, acid chloride etc. But…

(a) Circle the two compounds that are not carboxylic acid derivatives. Circle only two. CONHCH NOH NH COCI (b) Circle the two compounds that can be hydrolyzed to a ketone in aqueous acid. Circle only fwo. HC-N CO,Et (c) Circle the two compounds that can be converted to an aldehyde by reduction using DIBAL (also known as DIBAL-H). Circle only two. сно COEt (d) Cirele the two most reactive compounds with water. Circle only two OMe `NH2 CH,CH,CN (e) Circle the strongest acid. [2 marks] COH cOH COH `NO2 HC CHO "NO2 (1) Cirele ethyl benzoate and maleic anhydride. COCHCH, CO,CH,CH (g) Circle the two compounds that can be reduced to an amine using NaBH4. Circle only two. CH NH NH

(a) Circle the two compounds that are not carboxylic acid derivatives. Circle only two. CONHCH NOH NH COCI (b) Circle the two compounds that can be hydrolyzed to a ketone in aqueous acid. Circle only fwo. HC-N CO,Et (c) Circle the two compounds that can be converted to an aldehyde by reduction using DIBAL (also known as DIBAL-H). Circle only two. сно COEt (d) Cirele the two most reactive compounds with water. Circle only two OMe `NH2 CH,CH,CN (e) Circle the strongest acid. [2 marks] COH cOH COH `NO2 HC CHO "NO2 (1) Cirele ethyl benzoate and maleic anhydride. COCHCH, CO,CH,CH (g) Circle the two compounds that can be reduced to an amine using NaBH4. Circle only two. CH NH NH

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

For each of the given reactions, pick the correct description and the correct reagent.
5. Identify the type of each compound based on the function group it contains. (EOCQ 60) Compound Type of compound CH3-CH2-CH-CH2-CH3 Amine e.g NH2 нонн a. н-с-с-с-С-н H. нн CH3-CH2-CH2-NH2 CH3-0-CH3 С. HHHH O IIIII Н-С-С-С-С-С-ОН d. H HHH е. CH,-C-O-CH, f. CH3-CH2-CH2-NH2 g. H-C-C CH,CH, h. HICIH b.
The product of the reaction shown below is a(n). carboxylic acid imine amine amide H₂C CH₂ CHÍNH, NCH₂ CH₂
3) Name/Draw the following Carboxylic Acids Br a) (E)-5-methylhex-3-enoic acid
Draw the acid catalyzed hydrolysis of the following two compounds. Your products should be a carboxylic acid and an amine or alcohol. N за
I know that the 3rd one (second on the right side) has the highest pka because it's an alcohol and an alcohol is less acidic than a phenol. but I don't understand which compound has the lowest pka (strongest acid)?
Classify each reaction as either a proton transfer reaction, or a reaction of a nucleophile with an electrophile. Use curved arrows to show how the electron pairs move.
Draw the carboxylic acid product of the acid hydrolysis of methanamide, shown here. || H-C-NH2
1 / 4 124% 2. Draw the structures of the following compounds. a) acetonitrile b) formic acid c) benzophenone 3. Circle any acetal carbons in this molecule. но OH OH 4. Circle any hemiacetal carbons in this molecule.T CH HO OH
3. Circle the stronger acid between each of the following pairs of carboxylic acids. он но H. он он or or Br он or он or он но он но
How could one convert an aldehyde to a carboxylic acid? Group of answer choices- Reduce the aldehyde with hydrogen gas (H2) Oxidize the aldehyde using a mild oxidizing agent (such as permanganate). Combust the aldehyde with molecular oxygen. Use any of the above; each one would work OK.
from the three compounds on the left side, identify which one is most nucleophilic and which one is most basic.