Time left 0Which of the following acid derivatives can be hydrolyzed in water spontaneously withoutacid or base cotalysis?O BenzonitrileBenzamideO Benzoyl chlorideO Methyl benzoateWhich of the following compounds is lecast reactive in the nucleophilic aromatic substitutiorreaction with NaOH?

Given options are : a). Benzonitrile b). Benzamide c). Benzoyl chloride d). Methyl benzoate…

Answered: Which of the following acid derivatives…

Which of the following acid derivatives can be hydrolyzed in water spontaneously without acid or base catalysis? O Benzonitrile O Benzamide O Benzoyl chloride Methyl benzoate

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter19: Eas: Electrophilic Aromatic Substitution

Section: Chapter Questions

Problem 35CTQ

See similar textbooks

Related questions

Q: The reaction of 1-bromohexane with potassium cyanide will produce a(n) __________.

A: Given :- 1-bromohexane + Potassium cyanide → To determine :- Class of compound that will be…

Q: this drug contains one or more building blocks derived from either ethylene oxide or…

A: Drug Synthesis requires every sort of organic reagent present in the laboratory.

Q: Write the mechanism for the following reactions:1. the acid-catalyzed hydrolysis of an imine to a…

A: Introduction: An imine is a functional group having carbon-nitrogen double bond and enamine is a…

Q: Write a structural formula for the imine formed in each reaction

A: The reaction of ketone with primary amine in the presence of an acid catalyst leads to the formation…

Q: The indicated ester can undergo hydrolysis by either a chemical or an enzymatic process. Show the…

A: In the above reaction, ester Hydrolysis takes place. One base catalysis chemically and one is…

Q: Upon reacting with benzenesulfonyl chloride in Hinsberg's test, which of the following will form an…

Q: Define the following reagents or functional groups as being related to either aldehydes/ketone AK,…

A: Reagent have multiple character i.e selectivity and reactivity . Example :- LiAlH4 is a strong…

Q: What sequence of reactions would allow a conversion of an ester to an anhydride? NaOH SOCI, NaOH…

Q: Which of the following is a reasonable retrosynthetic approach to the target compound? он MgBr OH Br…

A: Free alcohol may hamper a Grignard reaction. So during retrosynthesis we have to very cautious…

Q: Rank the carbonyl-containing compounds in order of reactivity towards nucleophilic attack. Most…

Q: Show reagents and experimental conditions by which oxanamide can be synthesized from butanal.

A: The synthesis of oxanamide from butanal with reagents and experimental conditions is shown as…

Q: Which of the following is the appropriate reactants for the synthesis of pyrrole derivative below.…

Q: Identify the reagents that can be used to covert benzene into each of the following compounds:…

Q: Draw the structure of the major product formed in the following reaction when the aromatic aldehyde…

A: The methoxide ion acts as a base and deprotonates the methyl acetate to form the enolate ion. The…

Q: For the following synthesis of guaifenesin, identify the nucleophile and electrophile. Name one…

A: Given reaction:

Q: Draw the structure of the product/s in each of the following reactions. Ethanoyl chloride (A) Acetic…

Q: Which of the following carboxylic acid derivatives is the least reactive towards a nucleophilic…

Q: Which of the following carboxylic acid derivatives is likely to be least reactive with respect to…

A: The carboxylic acid contains -COOH functional group. The derivatives of the carboxylic acid will…

Q: Which of the following is expected to be the MOST reactive towards electrophilic aromatic…

A: Two questions base on introduction to organic chemistry that is to be accomplished.

Q: NH2 NHCOCH3 H/H2O (Hydrolysis) NO2 ÑO2 p-Nitroacetanilide (major) p-Nitroaniline

Q: Which of the following functional groups will react faster and at lower conditions to a nucleophilic…

A: Given Choices a. Carboxylic acid b. Nitrile c. Acyl Halide d Ester Functional Group will react…

Q: Amines possess the basic amino group that allows them to act as either bases or as nucleophiles.…

Q: List the following esters in order of decreasing reactivities towards hydrolysis with reason:…

A: In hydrolysis reaction, water molecule is added to the substrate. Esters can be converted to…

Q: Which of the following will not convert 1-butanol to 1- chlorobutane in one step? Cl4 PCI3 HCI SOCI2…

A: Given : Different - different compounds or reagents. To find : reagent that will not convert…

Q: Arrange the following compounds in order of decreasing reactivity towards hydrolysis. H2N. H3CO NAI…

A: A question based on reactivity towards hydrolysis reaction, which is to be accomplished.

Q: Which of the following sets of reagents would not be an acceptable method for the preparation of…

Q: In the Friedel-Crafts acylation (acid chloride), which of the following can serve as the active…

A: The question is based on the concept of organic reactions. we have to identify the correct…

Q: What will be the right combination of reagents to be required for the synthesis of the following…

A: In this question we can note that the formed mixture is an amine and an aldehyde. This can be form…

Q: What is the difference between the catalyzed and uncatalyzed preparation of acetanilide (acetic acid…

A: When acetanilide is prepared by reacting between aniline and acetic anhydride then here…

Q: Predict the major products when the following compounds are treated with Question #7…

Q: this drug contains one or more building blocks derived from either ethylene oxide or…

A: Certirizine has three building blocks derived from ethylene oxide, shown below, and can be…

Q: Which of the following correctly represents an intermediate step in the synthesis of a hemiacetal?…

A: Note: The questions which were posted consist of two different concepts, kindly post the second…

Q: Which reactant will give the products shown below when subjected to acid hydrolysis?

A: Hydrolysis of cyclic ketal results in the formation of corresponding ketone and a specific diol.

Q: . Show a reasonable mechanism for the following reaction. benzoic acid 1. NaOH 2. chloroethane ethyl…

Q: Q3/ Complete the following reactions : NaOH 1) 2-pantanone benzaldehyd + NaOH 2) hexanal +…

Q: Arrange the following compounds in an increasing order of their reactivity in nucleophilic addition…

A: Given, ethanal, propanal, propanone, butanone.

Q: On the basis of retrosynthetic analysis, identify starting materials and synthons for the following…

A: The retrosynthesis is generally a process of disconnecting the target molecules into synthetic…

Q: Identify the hydrolysis product of the cyclic enamine below 1) H30* 2) NaOH Ph The compound below Ph…

A: Option c is correct

Q: Which of the following reactions will give diphenylmethanone? I) Benzoyl chloride + Benzene + AICI3…

A: The structure of diphenyl methanone is as follows:

Q: Preamble: A student chemist in an attempt to synthesise compound B from the aromatic aldehyde. Use…

A: Aldehyde and ketone reacts with ammonia gas because there is a partial +ve charge on carbon making…

Q: Cardiolipins are found in heart muscles. Draw the products formed when a cardiolipin undergoes…

A: The mechanism is as follows:

Q: In the mid-1930s a substance was isolated from a fungus that is a parasite of ryes and other…

A: Given that, lysergic acid diethylamide (LCD, C20H25N3O). It is a weak base, having Kb = 7.6×10-7.…

Q: Which of the following sets of reagents would not be an acceptable method for the preparation of…

A: Please find your solution below : Ethyl acetate comes under the category of organic compounds called…

Q: The following product can be made from the reductive amination of which combination of compounds?…

Q: Please indicate which is the most acidic compound in each of the following pairs: thank you…

A: Most acidic compound in each of the following pairs =? 1) p-Nitrophenol and m-nitrophenol 2)…

Q: Which of the following reactions will NOT work to provide propyl butanoate as a product? OH OH H2SO4…

A: i think option - 3rd is the preferable choice that will follow the question requirement amide to…

Q: 2) Which of the following amine gives more faster addition and substitution reaction with the…

A: Cyclohexylamine reacts faster than aniline

Q: this drug contains one or more building blocks derived from either ethylene oxide or…

A: A skeletal and skeleton of a mole cure of organic compound is a type of molecular structure formula…

Q: this drug contains one or more building blocks derived from either ethylene oxide or…

A: Ethylene oxide is also called oxirane which is a three membered cyclic ring containing an ether…

Question

Time left 0
Which of the following acid derivatives can be hydrolyzed in water spontaneously without
acid or base cotalysis?
O Benzonitrile
Benzamide
O Benzoyl chloride
O Methyl benzoate
Which of the following compounds is lecast reactive in the nucleophilic aromatic substitutior
reaction with NaOH?

Expert Solution

This question has been solved!

Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.

SEE SOLUTION Check out a sample Q&A here

Step 1

VIEW

Step 2

VIEW

Step by step

Solved in 2 steps

SEE SOLUTION Check out a sample Q&A here

Knowledge Booster

Learn more about

Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.

Similar questions

Acetoxybenzene (PhOC(=O)OCH3) is much less reactive than ethoxybenzene (PhOCH2CH3) in electrophilic aromatic substitution reactions. Suggest an explanation for this result, based on an analysis of the inductive and resonance electronic effects of the two substituents on the stability of theWheland intermediate for para substitution by an electrophile E+
Propose a reasonable step-by-step mechanism for the following reaction.
Like other strong nucleophiles, triphenylphosphine attacks and opens epoxides. Theinitial product (a betaine) quickly cyclizes to an oxaphosphetane that collapses to analkene and triphenylphosphine oxide.(a) Show each step in the reaction of trans-2,3-epoxybutane with triphenylphosphine togive but-2-ene. What is the stereochemistry of the double bond in the product?(b) Show how this sequence might be used to convert cis-cyclooctene to trans-cyclooctene
Like other strong nucleophiles, triphenylphosphine attacks and opens epoxides. Theinitial product (a betaine) quickly cyclizes to an oxaphosphetane that collapses to analkene and triphenylphosphine oxide.(a) Show each step in the reaction of trans-2,3-epoxybutane with triphenylphosphine togive but-2-ene. What is the stereochemistry of the double bond in the product?
Which of the following is most susceptible towards nucleophilic aromatic substitution?
Multi-step synthesis. Give the reagents over the arrows and the intermediates between thearrows that are required to synthesize the product compound on the left from the reactant givenon the right for each retrosynthetic analysis.
Complete the electrophilic aromatic substitution mechanisms with the necessary substances!
What are the steps of the mechanism of reaction . Electrophilic aromatic substitution. Is it Ortho,para,meta ?
Please explain the synthesis. Identify SN1, SN2, E1, E2, nucleophiles and ekectrophiles.
Muscone synthesis is possible via an intramolecular Prins reaction. The starting point is cyclododecatriene, which his subjected topartial ozonolysis.With one aldehyde group protected,the other is reacted with isobutenyl magnesium chloride, and the protecting group is hydrolysed off. Then follows what is formally a Prins reaction,and etherification results in cyclisation to the bicyclic dihydropyran. Hydrogenation (at high T) finally gives racemic muscone. a. How to remove the protective group? b. What happens if you don't use a protective group?
Muscone synthesis is possible via an intramolecular Prins reaction. The starting point is cyclododecatriene, which his subjected topartial ozonolysis.With one aldehyde group protected,the other is reacted with isobutenyl magnesium chloride, and the protecting group is hydrolysed off. Then follows what is formally a Prins reaction,and etherification results in cyclisation to the bicyclic dihydropyran. Hydrogenation (at high T) finally gives racemic muscone. a. What is the protective group used in the muscone synthesis above? b. What is the name of the reagent used as the protecting group? c. What groups are protected in the above muscone synthesis ?
Propose a reasonable mechanism for the following reactions