what will be the steps involved to yield the product in this reaction

Q: Name of Ionic Compound Cation Anion Formula of Ionic Compoun Sodium Hydroxide Na* Calcium Phosphate…

A: Cation: It is the species that has positive charges due to the lack of electrons. Anion: It is the…

Q: Curved arrows are used to illustrate the flow of electrons. Use the reaction conditions provided and…

A: When aniline and hydrochloric acid react to give anilinium chloride salt, which is soluble in the…

Q: Draw and specify the complete reaction mechanism to determine the product from the reaction and…

A: (R)-3-chloro-2,3-dimethylpentane is a tertiary halide and it involves SN1 reaction with…

Q: In polar process of the reactions Bond formation is unsymmetrical Bond breaking is homolytic O…

A: Polar reactions occur when two bonded atoms come apart, one taking more of the shared electrons than…

Q: The reaction between 2-methyl-2-pentanol and sulfuric acid to yield 2-methyl-2-pentene goes via what…

A:

Q: Br OH NaOH Ph

A: When a substrate containing acidic hydrogen is treated with strong base, it is deprotonated forming…

Q: Complete the reaction and provide a mechanism for the formation of the product Na OCH2CH3…

A: Organic reaction mechanisms:

Q: Select the starting material(s) (SM) that would be expected to give Q as the major elimination…

A:

Q: Draw the most stable resonance form for the intermediate in the following electrophilic substitution…

A: Electrophilic aromatic substitution reactions are the characteristic feature of benzene and other…

Q: Draw the major 1,2- and 1,4-addition products obtained in the reaction shown. Assume that both are…

A:

Q: For each organic reaction, say whether at equilibrium there will be more reactants than products (so…

A: Answer:Any specie that loses H+ ion in its solution is called as Bronsted-Lowry acid and the specie…

Q: Classify the following substituents according to whether they are electron donors or electron…

A: Note - Since the given question is a multiple question , hence I solved first question . according…

Q: Draw the mechanism and the energy diagram for the reaction shown below. Include any resonance…

A: The acidic hydrolysis of di-substituted alkyne produces a ketone.

Q: Complete the following reaction scheme. Pay attention to stereochemistry. OH H step 1 A step 2

A: In step 2 there is nucleophilic substitution reaction of second order that means there occur SN2…

Q: Br

A:

Q: HO HO 识货品说一说

A: If possible in the presence of heat decarboxylation can takes possible. If decarboxylation leads to…

Q: When Br2 adds to an alkene the final product is called a dibromide.

A: The reaction is an addition reaction of alkene.

Q: Draw the major 1,2- and 1,4-addition products obtained in the reaction shown. Assume that both are…

A:

Q: Rxn E кон

A: Cycloalkyl reactant whose elimination and substitution products are to be determined.

Q: Show the organic product formed when methyl propanoate is reacted with lithium diisopropyl amide,…

A: ester in presence of base form enolate and carry out cross clasisen condensation with other ester.

Q: Which compound will undergo elimination-addition reaction (benzyne mechan

A: Here we have to predict the aromatic compound which will undergo elimination- addition ( benzyne…

Q: Draw the most stable resonance form for the intermediate in the following electrophilic substitution…

A: This is an fridel craft acylation reaction...

Q: Draw the structure of the missing reactants, intermediates, or products in the following mechanism.…

A:

Q: Why does the carbocation rearrangement take place?

A: If in any reaction carbocations are formed, the +ve charge on carbon rearrange from one carbon to…

Q: This is the general mechanism of nucleophilic addition of aldehydes and ketones. H–Nu Nu: Nu-C-…

A: the progress of a reaction can be studied by the energy profile diagram of the reaction

Q: Consider the following reaction. CH3CH₂CH=CHCOH HCI CH3CH₂CH-CHCOH CI + CH3CH₂CH H O CHCOH H CI this…

A: The objective of the question is to draw the structure of the carbocation formed during the course…

Q: Determine the mechanism and product for the given reaction by adding atoms, bonds, nonbonding…

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Q: H,SO4 HO.

A: Given reaction is;

Q: Draw the most stable resonance form for the intermediate in the following electrophilic substitution…

A: This is an electrophilic aromatic substitution reaction.

Q: E ر

A: Defined as the state corresponding to the highest potential energy along this reaction coordinate.

Q: For each organic reaction, say whether at equilibrium there will be more reactants than products (so…

A: Whether equilibrium lies on the right side or left side depends upon the acidity of the reactant and…

Q: Show the reaction mechanism for the acid-catalyzed hydrolysis of methyl ethanoate. Clearly show all…

A: The acid catalyzed hydrolysis of methyl ethanoate results in the formation of methanol and methanoic…

Q: 2. Propose a mechanism to account for the formation of this product. HO, H2SO4,Heat

A: When cyclopentylmethanol undergoes dehydration Reaction in presence of heat and sulfuric acid then…

Q: hok HBr

A:

Q: What is a multi-step synthesis for the following:

A: The final product can be prepared in the following steps:Step 1 : Preparation of alkene from alkyl…

Q: 1. Addition of HBr to alkenes occurs according to rule.

A: Alkenes are the class of unsaturated hydrocarbons. They have a general formula CnH2n. The carbon…

Q: I need a detailed reaction mechanism of this synthesis

A: Dear Student Find the complete Mechanism

Q: Using the curved arrow convention, write a detailed, step-by-step mechanism for the reaction of…

A: The explanation is given below-

Q: Give one example of elimination reaction (E2) type. Show the reactants materials and the product.…

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Q: In many reactions, warming the reaction mixture makes the reaction go faster. What is happening on a…

A: Collision theory of reaction rate: According to the collision theory of reaction rate, the randomly…

Q: draw the tetrahedral intermediate as it is ormed in the following reaction. H₂C. NH₂ HCI/H₂O reflux

A: The given reaction shows the acid-catalyzed hydrolysis of the reactant, amide to form carboxylic…

Q: Which of these functional groups is present in the major organic product of this reaction?

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Q: Question 15 What is not an expected product of the following allylic substitution reaction? NBS, hv…

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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.