Please choose the best answer possible. Thanks.
Correct answers
9. An Acid is correct answer
Because alcohol, Imine ,imide cannot form in hydrolysis.
10. In acid catalysed esterification of Acid and alcohol the mechanistic step is
Addition followed by Elimination.
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Please choose the best answer possible. Thanks. QUESTION 9 Which of the following can be made...
Question 17-17 What is the major organic product obtained from the following reaction? H2SO4 но он 3 но он но Question 17-30 Which of the following best describes the key mechanistic steps in the esterification of a carboxylic a upon treatment with an alcohol in the presence of a strong acid? a. addition followed by elimination b. substitution followed by addition c. elimination followed by addition d. addition followed by decarboxylation
Please choose the best answer for the following. What is the major organic product obtained from the following reaction? HCN, KCN ethanol, H2SO4, H20 water heat NH2 al 6.2 c. 3 d.4 Which of the following best describes the key mechanistic steps in the reaction of an acid chloride and an alcohol to form an ester? a. elimination followed by addition b. substitution followed by addition C. addition followed by elimination d. addition followed by decarboxylation
Which of the following can be made by acid-promoted hydrolysis of a nitrile? 1. an acid 2. an alcohol 3. an imine 4. an imide a. only 1 b. only 1 and 2 c. only 2 and 3 d. only 4 ANSWER: a can you explain why answer b,c,d are wrong please ?
Question 2 (1 point) Saved Which set of hydrogen atoms will undergo deuterium exchange with MeOD in the presence of MeONa? 1 2 1 and 2 only O2 and 3 only O 2 only O 3 only Which would be a reasonable intermediate for the this reaction? H30* PhoMe Ph-Me Ph Ome PhẩOMe OH PhẩOMe + OH OH + H2 Question 4 (1 point) Which hydrogen is most acidic? ace OD Question 5 (1 point) What is the product of...
QUESTION 36 Which would be the best substrate for a reaction that involves heterolysis? bromobenzene bromobutane 2-bromopropene benzyl bromide QUESTION 37 Which nitrile would form fastest in a substitution reaction of an alkyl tosylate with cyanide in a polar aprotic solvent 2-methylpentanenitrile 2.2-dimethylpentanenitrile pentanenitrile 3-methylpentanenitrile QUESTION 38 QUESTION 38 Which compound would have an odd molecular ion peak in the mass spectrum? O trichloromethane 1.1.2-trifluoroethanol ethylene oxide butan-2-amine QUESTION 39 How many products would result from the benzyne reaction (Na/NH3)...
Que. 24) What is the major organic product obtained from the following reaction? OH = ON Ph OH WN - d. 4 Que. 25) What is the best choice of reagent(s) to perform the following transformation? Reagents OH OCH a. CH3OH, H2SO4 b. CH31, H2SO4 C. NaOCH3 d. CH3Li Que. 26) What is the best choice of reagent(s) to perform the following transformation? OH он a. 1. LiAIH4; 2. H30+ b. H₂, Pt c. 1. NaBH4; 2. H2O d. NaH...
can you please solve question 89 both a and b part thank you Problems 787 What product would you expect to obtain from each of the following reactions? OH OH HC OCH2CH3 -CH2OH HCI The reaction of a nitrile with an alcohol in the presence of a strong acid forms an N-substituted amide. This reaction, known as the Ritter reaction, does not work with primary alcohols. RCEN + R'OH HCI R the Ritter reaction NHR a. Propose a mechanism for...
Question 17 (1 point) Ethers can be prepared from alcohols by? O a reductive addition. O an oxidative addition. O a nucleophilic substitution. O an electrophilic addition. O a condensation. Question 15 (1 point) Which reaction cannot be used to prepare an alcohol? addition of H30+ to an alkene. O an Organocuprate with an alkyl halide O a Grignard reagent with an aldehyde. O a Grignard with an ester Oa Grignard with a ketone Question 16 (1 point) Fischer esterification...
Question 26 (1 point) Saved Which best describes this transformation? Meo, CO Me Et Et NaoMe (2 equivalents) MeOH + H2NNH2 HNNH O 2 intermolecular nucleophilic acyl substitutions An intermolecular followed by intramolecular nucleophilic acyl substitutions O 2 intramolecular nucleophilic acyl substitutions O An intramolecular followed by intermolecular nucleophilic acyl substitutions Question 27 (1 point) What is the product of this reaction sequence? 1. NaOEt 2. BrCH_CH_CH_Br (0.5 molar equivalent) 3. NaOEt 4 H30*, Heat CH(COCH2CH3)2 -COH HOO.COM C.com HOC...
Multiple choice. Choose the best answer possible. Which of the following carboxylic acids undergoes the most rapid thermal decarboxylation reaction? wy POH OH 0 4 al 6.2 OC.3 O 0.4 What is the major organic product obtained from the following sequence of reactions? OEt OEU 2. H30* OOOO doo