(b) Discuss about the stability factors of the reaction intermediates, which involved in a name reaction "Wittig rearrangement".

Q: Give mechanism and write a complete Energy Diagram for Sulfonation of Benzene:

A: When the benzene is treated with conc. sulphuric acid, benzene sulphonic acid is formed. This is…

Q: Rank these nucleophiles from most to least reactive for substitution reactions and give a brief…

A: The nucleophilicity of a species depends on various factors such as negative charge density,…

Q: g. CH3 H3C-CH CH-CH3 OH Stereochemistry:R H3PO4 Major Product(s) of Reaction g

A:

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: 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: NO2 + Br2 with FeBr3

A: The given reaction is an example of an aromatic electrophilic substitution reaction. Nitrobenzene…

Q: Outline the synthesis of 1-bromo-2-methylpropane by using suitable alkene

A:

Q: . Aldol addition of mo-on-on XS H3C-CH2-CH2-C-H "OH Major Product of Reaction i +

A:

Q: Give the MAJOR product(s) for the following reactions. For example, if BOTH elimination and…

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

Q: Give the product of the mentioned reaction. Give clear handwritten mechanism of reaction!

A: Ozonolysis of alkene: One of the important reactions of alkene is ozonolysis. In the ozonolysis…

Q: Compare Electrophilic aromatic substitution reactivity to quinoline and isoquinoline. Please,…

A: Quinoline/isoquinoline - attack at 5,8 benzene positions 5 membered rings - electron rich, readily…

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

A:

Q: Give the MAJOR product(s) for the following reactions. For example, if BOTH elimination and…

A: We will write the final products of the all reactions

Q: plain the principle of 'Using Safer solvent taking suitable ample of a conventional reaction and its…

A:

Q: and all of the intermediates in a synthesis similar to the one just given that relates the…

A: In the sequence, (-)-Glyceraldehyde reacts with HgO to form (+)-Glyceric acid with the elimination…

Q: 9. By employing our understanding of nucleophiles and electrophiles, as well as kinetics and…

A: “Since you have posted a question with multiple sub-parts, we will solve first three subparts for…

Q: a. Label the reactive features of the following reactants, select the most reactive feature, then…

A: The organic reactions take place in more than one step with the help of reagents.

Q: n. CH3 H;C-CH-CH-CH, TSCI ОН CH,O Stereochemistry: R Major Product(s) of Reaction n Stereochemistry…

A: S only as the reaction undergoes via Sn2

Q: Give the MAJOR product(s) for the following reactions. For example, if BOTH elimination and…

A: We will write the products of the reaction

Q: A compound X on reductive ozonolysis gives ethanal, methanal and carbon-dioxide. X is

A: Ozonolysis is the reaction of alkenes with ozone to form aldehydes and ketones. The given products…

Q: CH3 H3C-CH-CH-CH3 ОН Stereochemistry: R HBr Mаjor Product(s) of Reaction а b. H3C-CH2- -H…

A: Introduction: Substitution reaction: When one functional group of a compound replaces the other…

Q: 9. By employing our understanding of nucleophiles and electrophiles, as well as kinetics and…

A: The kinetically favored product and thermodynamically favored product is formed at low temperature…

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: Consider the reaction: Provide the missing reagents [A) and [B). Explain why aqueous acid must be…

A: At first 2-Bromo propane is treated with A. Mg/Et2O to give isopropyl magnesium bromide. Here,…

Q: Consider the following incomplete photochemical pericyclic reaction. hu Draw the structure of the…

A:

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: Give the MAJOR product(s) for the following reactions. For example, if BOTH elimination and…

A: In this question, we want to write intermidiate Product and final product of this reaction.

Q: A.With equations,state the limitations of friedel crafts acylation and alkylation. B.State the…

A: SOLUTION: Step 1: The limitations of Friedel – crafts alkylation are as follows: Alkyl halides like…

Q: Explain the benzyne mechanism.

A: Benzyne is an reaction intermediate which will formed by reaction of halobenzene with strong base at…

Q: Explain why compound A will not undergo a ring-opening reaction under thermal conditions, but…

A: Ring opening reactions for A and B are given below :

Q: Give the reaction mechanism (showing curly arrows) for the bromination of methane in the presence of…

A: Organic reactions are those in which organic reactant react to form organic products.

Q: Which compound (i or ii) is the stronger base? Discuss your answer comprehensively by amoungst other…

A: 1- (II) compound is less basic because it's having benzene ring on para-position which act as…

Q: How many elimination product(s) is /are possible in the reaction of compound…

A: Here, we have to find the number of elimination products that are possible in the reaction of…

Q: Provide the structure of the product(s) with stereochemisty if appropriate. If multiple products…

A: Indicate major product of Given reaction

Q: Explain why free-radical halogenation usually gives mixture of products.

A: Consider free radical halogenation of Alkanes. They undergo this reaction in the presence of light…

Q: Arrange the compounds in increasing order according to its stability of carbocation

A:

Q: b) Provide a stepwise mechanism for the bromination of nitrobenzene.

A: -NO2 is a electron withdrawing group,it pull electron from ortho and para position by resonance and…

Q: (b) Complete the following reactions and suggest plausible mechanism. Mention the step where the…

A: The Answer Of the Following Questions are given as below:-

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: Give the MAJOR product(s) for the following reactions. For example, if BOTH elimination and…

A: The given reaction is an example of elimination reaction.

Q: Write the mechanism for the nitration of toluene showing explicitly why ortho and para products are…

A: We have to show mechanism for nitration of toluene showing why ortho and para product favoured over…

Q: Give the reaction mechanism (showing curly arrows) for the bromination of methane in the presence of…

A: Here we are required to show the mechanism of the reaction

Q: Differentiate between stereoselective and stereospecific reaction and apply this knowledge on…

A: Stereospecific reaction : A reaction in which only one stereoisomer is allow to be formed.…

Q: H CH3 + "OCH3 Major Product(s) of Reaction k (Show appropriate stereochemistry representations.) он…

A: Given reactions are the elimination and substitution reactions.

Q: Give

A: We have to give product of the given reaction

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.