List TWO nucleophiles that would react with the epoxide belowwith the opposite regioselectivity compared to aqueous acid.

Q: You have learned two ways to make an alkyl benzene: Friedel–Craftsalkylation, and Friedel–Crafts…

A: Alkyl benzenes are the substituted benzene in which substituent is an alkyl group. Benzene undergoes…

Q: Draw the structure of the product for each of the following mechanistic steps.

A: The products of the given mechanistic steps can be written by following the arrows drawn.

Q: Enamines can serve as enolate surrogates in reactions at the a-carbon. In the following reaction…

A: An enamine is an unsaturated compound derived by the condensation of an aldehyde or ketone

Q: Which one of the molecules shown below prefers to exist as its enol tautomer?

A:

Q: Draw the structure (including stereochemistry) of an alkyl chloride thatforms attached alkene as the…

A: The alkyl chloride should be such chosen that it forms the product as the one and only major…

Q: Which of the following is most susceptible towards nucleophilic aromatic substitution?

A: The aromatic nucleophilic substitution reaction follows addition elimination mechanism.

Q: The conversion of acid anhydrides to ester via alkoxides is a favorable reaction

A: A question based on introduction to organic chemistry that is to be accomplished.

Q: Which of the following dihalides is/are an appropriate substrate, when treated with a strong base…

A: To solve this problem we have to convert dihalides into  an alkyne .

Q: Write the detailed mechanism for the following tranformations.

A:

Q: Which ion in each of the following pairs is a better leaving group?Explain answer briefly

A: Leaving group is the species that get removed with a pair of electrons in a heterolytic bond…

Q: What is the slow (rate-determining) step in any electrophilic aromatic substitution reaction? Please…

A: Please find below a example of the reaction mechanism

Q: Which of the following alkyl iodides would react fastest in the different reaction mechanisms given…

A: General order :-  For SN2 reaction:-  Methyl>1°>2°>3°  3° alkyl halide is so crowded that…

Q: Supply the structures of reactant(s) or product(s) for the following aldol and Claisen reactions

A:

Q: The by-product of the aldol reaction is not drawn here, what is it?

A:

Q: Is it possible to regioselectively form one or the other enolate by the proper use of reaction…

A: Regioselectivity: When two organic compounds react, the preference of one compound to form or break…

Q: nucleophile

A:

Q: Draw the major organic product of the reaction.

A: This a Grignard reaction, epoxide react with Grignard reagent to form the corresponding product.…

Q: What is the major neutral organic product for the following sequence?

A:

Q: DHG (OACameay

A: The above-given reaction is an example of Oxymercuration demarcation reaction:

Q: Why alkyl halides are considered to be very reactive compounds towards nucleophile? they have a…

A: Introduction: We have to explain which is correct statement for the above question.

Q: In an unsymmetrical epoxide, the nucleophile attacks at the lesssubstituted carbon atom. Explain…

A: In an unsymmetrical epoxide, the nucleophile attacks at the less substituted carbon atom because of…

Q: What is the appropriate electrophile nucleophile and solvent to achieve this final product

A:

Q: Provide the MAJOR product of the following reaction and draw the curved-arrow

A: Regiochemistry is the chemistry of regioselective reactions Regioselectivity is the priority of…

Q: In both examples below the reactants shown are combined to bring about a nucleophilic substitution…

A: If weak base is used (dil.NaOH), substitution reaction takesplace  Benzyl chloride undergo SN1…

Q: Draw structures for the carbonyl electrophile and enolate nucleophile that react to give the enone…

A: Given: product

Q: Draw the structure of the following thiols, thioethers, and missing product of reaction. Use the…

A: Structure of Compound and  Product Formation mentioned in step-2

Q: When naphthalene undergoes an irreversible electrophilic aromatic substitution, such as a…

A: Alpha position is more stable than beta position because

Q: What is the major organic product in the following sequence of reactions?

A: Major product:

Q: Select the major product of the following reaction.

A: Electrophilic addition reactions (EAR):  In general alkenes undergo electrophilic addition…

Q: How Reactivity Depends on the Basicity of the Leaving Group?

A: Applying basic concepts of relationship between  leaving ability and base character of leaving…

Q: Illustrate the steps of a directed aldol reaction between a ketoneand an aldehyde, both of which…

A: Aldol reaction: It is reaction occurs between aldehydes, in which β hydroxy aldehyde (aldol) is…

Q: In the mechanism for electrophilic aromatic substitution with a diazonium ion as the electrophile,…

A: We can use the concept of hard and soft acid and base. The terminal nitrogen atom of the diazonium…

Q: Which ester, C or D, is more reactive in nucleophilic acyl substitution?Explain your reasoning.

A:

Q: Explain why one of the following molecules will undergo an E1 elimination faster:

A: In the E1 reaction the elimination of leaving group first and then deprotonation takes place finally…

Q: Show the detailed mechanism of the Fischer Esterification reaction that will be involved in the…

A:

Q: Examine

A: We will write the required information

Q: Question attached

A: The bimolecular nucleophilic substitution reaction is a single step reaction which proceeds via the…

Q: Which one  would be most reactive toward electrophilic aromatic substitution?

A: Aromatic electrophilic substitution reaction: Aromatic electrophilic substitution reactions are the…

Q: Predict the most likely sites of electrophilic aromatic substitution in each of the following…

A: Predict the most likely sites of electrophilic aromatic substitution in the above molecules are…

Q: Draw the product of (S)- propene oxide and hydrogen chloride in diethyl ether Could you explain why…

A: We have to draw the product of (S)- propene oxide and hydrogen chloride in diethyl ether. Could you…

Q: Any base whose conjugate acid has a pKa greater than ______ can remove a proton from a terminal…

A: In the formation of acetylide ion by removing a proton from the terminal alkyne, base used to remove…

Q: Rank the following alkyl chlorides in order of reactivity (fastest to slowest) in the SN2 reaction…

A: The SN2 reaction proceed by the concerted mechanism, that is, leaving group will leave and entering…

Q: What are the nucleophilic strengths in descending order of the nucleophiles in protic and aprotic…

A: A good nucleophile is the one that can donate lone pair of electrons.

Q: Give the major organic product for each step of the following reaction

A:

Q: Order of reactivity towards nucleophilic substitution reaction of the compounds

A: Order of the reactivity towards nucleophillic substitution reaction of the compound

Q: Draw the organic product (if any) expected from each of the following oxidation reactions

A:

Q: Determine whether attached nucleophilic acyl substitution is likely to occur.

A: Nucleophilic substitution reaction involves the substitution of a leaving group by a nucleophile.…