sider the following reaction.

Q: redict the major product for the reaction shown.

A:

Q: And which one is the major product?

A: To explain: The major product?

Q: (SYN) Show how to carry out the following conversion.Hint: Consider using a protecting group.

A: Given reaction,

Q: ion was found to E he reaction rate to fo

A:

Q: Draw the mjor product of both question with mechanism asap

A: Given structure of reactants.

Q: Draw the all the products. Add non‑bonding electrons where applicable.

A: This reaction is an example of epoxide ring opening.  In basic medium nucleophilic attack happens at…

Q: c) Circle the most electrophilic carbon in the structure below and explain your choice.

A:

Q: Follow the curved arrows and draw the products of the following reaction. Include all lone pairs and…

A:

Q: duce this regiochemistry in elimination reaction. Br

A: As we know,  In E2 mechanism polar aprotic solvent is required and strong base and heat is also…

Q: Which product(s) will predominate if the reaction is under kinetic control?

A: According to the reaction mechanism or temperature dependence. Two types of products are formed in…

Q: What is product E, and draw the structure

A:

Q: Follow the curved arrows and draw the products of the following reaction.

A: The reactants are protonated form of cyclohexanone and a ethane-1,2-diol . This acid catalysed…

Q: Provide a Curved Arrow Mechanism for the following reaction. .CI HO- HCI

A: The above reaction is an example of a substitution reaction where the reaction goes through a…

Q: Substitution with a(n) to an aromatic ring would result in reaction? Deactivator group, fast…

A: Activator - electron donating group  and para and ortho directing  Example - OH, OCH3 Deactivator -…

Q: Problem: Consider the reaction sequence shown below. Pay attention to stereochemistry. (a) Draw the…

A: Ans

Q: Draw the product of attached reaction ?

A:

Q: Which of the following reagents can do conjugate addition?

A: A conjugate addition with a nucleophile as carbanion (C-) is known as the Michael addition or…

Q: H H H-O- ċ-H + :Br: н — Br : : OH : - -

A: In SN2 reaction, the nucleophile attacks on the substrate from the back side of leaving group and…

Q: ct the product f

A:

Q: Q7. Propose a detail mechanism for the following reaction. Use curved arrow to show the electron…

A: Alcohols are the organic compounds which contains an -OH group in it. It undergoes dehydration in…

Q: or each addition route of the reaction, draw the structure(s) of the major product(s), including…

A: Answer of the question given below,

Q: Problem: Consider the reaction sequence shown below. Pay attention to stereochemistry. (a) Draw the…

A: Concentrated H3PO4 is a dehydrating agent, and with secondary/tertiary alcohols, form alkenes. With…

Q: e product(s

A:

Q: Rank the nucleophile strength of the compounds below from weakest to strongest

A: A nucleophile is defined as a chemical species that can donate its electron pair. So, it is cleared…

Q: Draw ths missing curved arrow notation for the E2 reaction. AV

A: The secondary and tertiary alkyl halides proceed with E2 mechanism in the presence of base HO- .…

Q: Consider the following step during free radical substitution reaction. CH3 + CI• > → CH;CI What is…

A: Correct answer is Termination. It is the termination step of the reaction free radical substitution…

Q: Draw the product of attached reaction

A: Organometallic reagents are very useful in the field of chemistry as they can make a variety of…

Q: AICI

A:

Q: e problem to get the product shown. CI AICI3

A: The question is based on the concept of electrophilic substitution reaction . We have to account for…

Q: Br2 undergoes electrophilic addition to maleic anhydride as shown here. Explain why this reaction is…

A: Here in this compound the C=C double bond is resonance stabilized by two keto group adjacent to…

Q: Which sn² reaction is each pair is faster

A: Given Two SN2 reactions varied by two different nucleophiles OH- and CH3COO-

Q: so, Cl, H,SO, AICI,

A: The reactant, benzene is treated with SO3/H2SO4 first and then Cl2/AlCl3.  We have to predict the…

Q: Carbocation rearrangement of the cation on the right gives: A) B) D) two of the above

A:

Q: For the reaction below: OTs KCN DMSO Draw the major organie product(s) in the sketch pad below.

A: OTs is an extremely weak base and a good leaving group. KCN with DMSO leads to cyanation by a…

Q: AICI,

A: Using concept of fredalcraft acylation ,this can be determined.

Q: Follow the curved arrows and draw the products of the following reaction. Include all lone pairs and…

A: We need to draw the products of given step of mechanism of reaction.  The curved arrow in mechanism…

Q: from b.

A: For this transformation, oxidation of the alkene is carried out.

Q: 4.2 Draw the product(s) of the following reaction by following the curved arrows.

A: Given incomplete reaction is : Draw the products of the reaction by following the curved arrows = ?…

Q: Name the following:

A: Rules :  1) identify the longest parent chain. 2) number them in such a way that the sum of number…

Q: а. Draw in any missing lone pairs b. Draw appropriate curved arrows to complete the acid-base…

A: All the three questions are answered in one chemical equation which is given on page

Q: EXTRA CREDIT: Complete the following two-step synthesis: ? ? ?

A:

Q: what is the plausible synthesis?

A:

Q: What will the formula be of the main produc

A: Answer is there is formation of ether  CH3OCH2CH2CH3

Q: najor product of the following reaction

A:

Q: prounde reagent tocary followngons tormation. out the

A: Answer is explained below.

Q: Which compound/s will react with Br2 in water under light conditions? May answer one or more…

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

Q: Same reaction as previous question. Which statement(s) is(are) true concerning the rate-limiting…

A: We have to predict the correct statement regarding rate limiting step.

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.