Provide the curved-arrow mechanism to account for the following nucleophilic addition- elimination reaction. 1. NaH

Q: We discussed a tetrahedral intermediate in the context of reactions of derivatives of carboxylic…

A: Let the general example can be taken as follows:

Q: Below is a schematic representation of possible reactions that Compound X can undergo. Use the…

A: The given reaction is the reaction where the cyclic alcohol reacts to give respective cyclic…

Q: Arrange the following radicals in order of decreasing rate of bromination. Justify your answer.

A: given     arrange the following radicals in order of decreasing the rate of bromination. The…

Q: Outline a stepwise mechanism for the following reaction: Br Br2 + HBr CH;COOH

A:

Q: Explain how Hammond's postulate accounts for the higher selectivity of bromination reactions as…

A: We have to explain how the Hammond postulate accounts for the higher selectivity of bromination…

Q: which is more basic?? pipyridine or pyridine  Explain with resonating structure?

A: According to Lewis definition of acid and base, a base is a substance that can donate a pair of…

Q: Write a mechanism for the following reaction

A: The details solution for this is provided below in attach image.

Q: QUESTION 1 provide a stepwise mechanism that accounts for its formation.

A: The following reaction is the conversion of 1-methyl-1-cyclohexanol to 2-methyl-cyclohexanone.

Q: Outline a feasible synthetic route for the following:

A: Step-1:  Free radical substitution reaction  Step-2: Nucleophilic substitution reaction

Q: What is the arrangement between the structures in the order of decreasing reactivity toward

A:

Q: Consider this scheme. Why does a ring form with a single ethylene glycol on A rather than two…

A: A single ethylene glycol on A rather than two molecules of ethylene glycol to form acyclic acetals…

Q: Which compounds are more nucleophilic, ethers or sulfides? Explain your answer and provide an…

A: The special group in an organic compound which decides the chemical properties is known as the…

Q: How many carbonyl groups are generated upon treatment of the molecule below with ozone, followed by…

A:

Q: Provide the curved-arrow mechanism to account for the following nucleophillic addition-elimination…

A:

Q: Provide a note on Peterson syntheses, with suitable example and mechanism.

A: Peterson synthesis is synthesis of olefinic double bond from carbonyl using α-silyl alkane.

Q: 3. It is required to introduce a halogen group to a five membered ring, thiophene. Discuss the…

A: When an atom of a cyclic hydrocarbon is replaced by a heteroatom such as nitrogen, oxygen, and…

Q: (b) Discuss about the stability factors of the reaction intermediates, which involved in a name…

A: The answer is as follows:

Q: When attempting to synthesize an alkyne, why is the hydrogen on the right abstracted instead of the…

A: This can be explained as:

Q: A- What is the definition of acidity? B- Compare the acidity of ammonia and its aliphatic…

A: As per rule i should have to answer only three subparts so please ask remaining in other post.

Q: ОН

A: These reactions are generally proceeds in a heating or light conditions.  Here we are given with…

Q: Define the General Mechanism–Acid-Catalyzed Nucleophilic Addition ?

A: A nucleophilic expansion response is a compound expansion response where a nucleophile structures a…

Q: Outline a stepwise mechanism of the following reaction: Br NHCH3 CH;NH2 NO2 ÑO2

A: Given  Reaction of  P-nitro Bromobenzene with Methyl amine  Mechanism = ?

Q: How many carbonyl groups are generated upon treatment of the molecule below with. ozone, followed by…

A: 8 carbonyl are form as general mechanism are shown below.

Q: Which of the following is a proper and reasonable resonance hybrid structure of benzaldehyde that…

A: When a molecule (or) ion can not be represented by single lewis dot structure and more than one…

Q: what is the alkene that would give the product ( a or b)?and why?

A: Alkenes are the compounds that contain at least one carbon-carbon double bond. These compounds…

Q: Suggest short, efficient reaction sequences suitable to produce the compound from the given starting…

A: In this question, we will synthesized the final product from the starting material which is alcohol…

Q: Place the following cyclic compounds in order from highest to lowest stability. For the lower…

A: cyclopropane and cyclobutane are less stable than cyclohexane, because the smaller rings are more…

Q: Explain and provide the mechanism of the reaction. Name the final product with the assignment of…

A: The mechanism for given reaction is shown below,

Q: Rank the following in order of increasingly exothermic heat of hydrogenation. Explain. A B

A: Enthalpy of hydrogenation is the amount of energy released when one mole of an unsaturated compound…

Q: Provide a plausible arrow pushing mechanism for the reaction below.

A:

Q: 1. Suggest a plausible arrow-pushing reaction mechanism for the following reaction. Clearly dictate…

A: Explained along with stereochemistry.

Q: 1. Explain the the following,giving examples and illustrations to support your answer Electrophilic…

A:

Q: 1) Which one more reactive to word nucleophilic substitution P- nitro toluene or O- ethyl toluene ?…

A: P-nitro toulene will be more reactive towards nucleophilic substitution than O-ethyl toulene because…

Q: Compound B undergoes the formation of the shown carbonation 100 times faster than compound A.…

A: Various intermediates are formed in organic chemistry. Their formation and stability depend upon…

Q: Provide the curved-arrow mechanism to account for the following electrophilic aromatic substitution…

A: Chlorination of benzene: This reaction is an example of an aromatic electrophilic substitution…

Q: Discuss the hybridization, aromaticity, and stability of the following organic intermediate. Also,…

A:

Q: Propose a curved arrow mechanism to account for the formation of compound C.

A:

Q: c) Rank the following compounds in order of increasing reactivity toward nucleophiles. Explain your…

A: There are many mechanisms in organic chemistry such as nucleophilic substitution, nucleophilic…

Q: b. Predict the product of the reaction between the enamine from part a and ethyl iodide. Hint:…

A: In this question we have to tell the product of the reaction.

Q: A ketone undergoes acid-catalyzed bromination, acid-catalyzed chlorination, racemization, and…

A: ketone undergoes acid-catalyzed bromination, acid-catalyzed chlorination, racemization, and…

Q: Nitrogenous Mustard has been used as an alkylating anticancer agent. Explain the alkylation feature…

A: Nitrogenous Mustard has been used as an alkylating anticancer agent. Nitrogen mustards are cytotoxic…

Q: 7. Outline a synthesis for each of the following alkynes, using any necessary organic or inorganic…

A: Given reactions:

Q: Provide all resonance structures of the sigma complex when aniline reacts with an electrophile to…

A: Reaction is taking place between aniline and Br2 (Br electrophile)

Q: Using the principles described in this course, explain (using sentences and drawings) why…

A: The more stable the carbocation ,the lower the activation energy for reaching that inter mediate…

Q: a. b. HBr, A Peroxide NBR, A Peroxide

A: In  reaction a)  Alkene is treated with HBr  in presence of peroxide which follows anti markonikov's…

Q: Arrange the following in order of decreasing reactivity to nucleophilic addition: ketone, aldehyde.…

A:

Q: Rank the indicated hydrogen atoms in order of increasing ease of abstraction in a radical…

A: The order of increasing ease of abstraction in a radical halogenation reaction will be based on the…

Amines

Amines are organic compounds with a nitrogen atom having a lone pair of electrons on it. They are derived from ammonia (NH3) wherein hydrogen atoms are substituted by an aryl or alkyl group.