Please Complete the following reaction with Major Compund with explaination in handwritten....

Q: The major product of the following reaction is он H,SO, heat

A: First lone pair of OH will attack on H of H2SO4. See the written solution.

Q: Write the complete mechanism with arrows of the following reaction. A

A: This reaction is a [1,3] cycloadditon reaction.The mechanism is as given below.

Q: i See Periodic Table See Hint Add curved arrows to this enol structure to show the formation of the…

A: The carbonyl compound shows keto-enol tautomerism. One form can be converted into another form in…

Q: Draw the major organic product of the reaction. Show the stereochemistry, if applicable. Omit…

A: Introduction: When an alkyl halide is treated with a nucleophile, it removes the halide ion. t-alkyl…

Q: ): In the space provided below please give the detailed mechanism for the following transformation.…

A: The reaction given is,

Q: The major product/s that form/s during the nitration of benzenesulfonic acid is?

A:

Q: Give a clear handwritten answer with explanation...give the mechanism of all sub parts  reactions…

A: 1) SN2 mechanism: Concerted mechanism with inversion of configuration 2) E2 mechanism: Concerted…

Q: at is the correct order of decreasing reactivity ost reactive first) of these compounds toward…

A: When electron donating groups are attached to benzene ring.so, they increase the reactivity towards…

Q: Provide to llaving Br a detailed, step by step mechanism for reaction OCH₂CH3 OCH₂CH3 OCH₂ CH3

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Q: Draw a reasonable synthesis for this reaction

A:

Q: Complete the following reactions, clearly indicating regio-and stereochemistry where applicable. In…

A: Reaction is given below.

Q: Give a clear handwritten answer...Give a synthesis mechanism for given below reaction...

A: We have to synthesis the given compound. We also have to give the mechanism of it..

Q: Complete the following transformation and provide the detailed steps

A: Aldehyde is protected using a protecting group and another aldehydic group is reduced to alcohol…

Q: CH3I EXcess

A:

Q: Rank the following species from best nucleophile to poorest nucleophile in an aqueous solution:

A: Nucleophilicity depends upon the tendency to donate electron pair. This tendency depends upon…

Q: Explain the synthesis of B-ionone. Also do the mechanism with explanation in details

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Q: O2N Br

A:

Q: х бон

A: We have to carry out the given synthesis. The required synthesis is shown below

Q: Increasing alkyl substitution stabilizes an alkene by an electrondonatinginductive effect. Explain ?

A: Alkene are hydrocarbon having carbon - carbon double bond . Increasing alkyl substituents ,…

Q: The attached reaction does not afford the major product that is given.Explain why this is so, and…

A:

Q: Give a clear explanation handwritten answer with textual explanation...give the mechanism of given…

A: The given reactant is a tertiary alkyl bromide which is an alkyl halide.  The reagent is KCN and the…

Q: nucleophilic

A: Dear student I have given answer to your question in the image format.

Q: please help with this question. thank you. Propose an efficient synthesis of for each of the…

A: 1. Alkenes upon ozonolysis to give carbonyl compounds , alpha hydrogen containing carbonyl…

Q: synthesize the above, respectively, starting with Se8.

A: The gain of electron is named as oxidation whereas loss of electron named as reduction. The reaction…

Q: a) electrophilic aromatic addition reaction C) nucleophilic aromatic addition reaction nucleophilic…

A: The question asks about the category under which the nitration reaction of benzene with HNO3 and…

Q: Please synthesize problem B and D starting from benzene.

A: There are different types of electrophilic substitution reactions - 1- halogenation 2- nitration 3-…

Q: Provide the missing reagent indicated by "???" CI ??? OH (+ other products)

A: Nucleophilic reactions are identified as of two types namely substitution and elimination. In the…

Q: Come up with a reasonable mechanism for the following reaction

A: In this question we want to draw reasonable mechanism for this reaction.  This reaction is Aldol…

Q: The following carbocation undergoes a rearrangement by a hydride shift as shown below. The reason…

A: Given, a carbocation which undergoes rearrangement by hydride shift  We need to explain the reason…

Q: Which of the following is the correct order of increasing reactivity in nucleophilic substitution…

A: Acid halides, esters , anhydrides, amides etc. are the carboxylic acid derivatives. Their reactivity…

Q: Give a clear handwritten answer with explanation..give the mechanism with explanation of given bleow…

A: In this question, we will see the reaction mechanism for the given transformation from the reactant…

Q: H.C.,

A: -> First of all in presence of methyl iodide methylation occur and quaternary ammonium salt…

Q: ome me

A: 1. Step 1 : Birch reduction. Step 2 : The starting material is treated with acid results…

Q: OTos Ph

A: Since OTos is a strong leaving group. Hence the reagent given above arrow will attack on the…

Q: Give a clear handwritten answer with explanation..give the mechanism of given bleow reactions...

A: Butyl lithium will acts as strong base, it abstract acidic proton resulting a nucleophile is…

Q: Give a clear handwritten answer..give the mechanism to given below reaction

A:

Q: the

A:

Q: from and alcohol of two carbon or less Cl

A:

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

A: Step 1: B). The type of reaction involved in both (i) and (ii) is dehydration of alcohol (removal of…

Q: Br2 light or heat

A: Given reaction is :  Complete the reaction and gives the major product of the reaction = ?

Q: Provide only one plausible retro synthetic scheme for the molecule below. In addition, provide a…

A:

Q: Because they are so often used as protecting groups in organic synthesis, the choice of which acetal…

A:

Q: 1.

A: Reaction 1 : Acid catalyzed esterification. Reaction 2 : C- acylation.

Q: the reduction of α-methylvaleraldehyde, results to?

A: Reduction of aldehyde give alcohol

Q: BuLi

A: Organolithium is a reagent that acts as a base or nucleophile in the reaction as per the given…

Q: Give a clear explanation handwritten answer...complete the following reaction

A: Dimethyl formamide is a polar aprotic solvent, thus the Reaction between a tertiary alkyl halide and…

Q: Give major product part a,b,c properly

A: Solution- major product of given below with there reaction;

Q: a. Explain the steps involve in the below organic reaction in detail ONa HON

A:

Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.