so, Cl, H,SO, AICI,

Q: 1. O3 g. 2. DMS for h. Na NH3 1. mCPBA 1. 2. H30* j. Cl2

A: Organic reaction mechanisms:

Q: From each pair, select the stronger nucleophile. Q.) CH3OCH3 or CH3SCH3

A:

Q: Draw a stepwise, detailed mechanism for attached reaction.

A: A detailed mechanism for the given reaction can be drawn as,

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

A:

Q: 1. Show how to carry out the following transformation. N ? N.

A: Note: Bromination of benzene. Acetylation of bromo benzene. Azo coupling. Sonagashira coupling.…

Q: HO What sequence of reagents can be used to accomplish the con

A: Following are the steps to accomplish the transformation 1. Free radical substitution to give alkyl…

Q: Draw a detailed mechanism showing the formation of all products, be sure to draw all intermediate…

A: Given reaction show mixture of ester and alkene as products. In first step of this reaction removal…

Q: (CH3),CCI ?

A:

Q: Show the detailed mechanism of this in 3D structure, and predict the major regioisomer and the major…

A: The hydration of the given compound [1] takes place and regioselectivity is decided on the basis of…

Q: Draw a detailed mechanism showing the formation of the product, be sure to draw all intermediate and…

A: Here I have shown a detailed mechanism of the reaction

Q: Draw all products, including stereoisomers, in the following reaction.

A: The given reactant is a 3° (tertiary) alkyl halide.

Q: Please identify major PRODUCT A and major PRODUCT B.

A: We have given the organic reaction and we have to identify major PRODUCT A and major PRODUCT B

Q: CN NaOH HO H20 NC

A: Solution :         NaOH and water used as a reagent.NaOH is a base that is used to abstract…

Q: Give the curved arrow mechanism for the transformation below CI H2N-NH2 NH pyridine NH

A: The answer is given as follows

Q: Starting from intermediate X, complete the mechanism. Provide curved arrows for both steps and draw…

A: The carbocation formed in the intermediate X is unstable because it is present at bridge head…

Q: MCPBA

A: The given reaction is the Baeyer-Villiger reaction where the mCPBA (meta-chloroperoxybenzoic acid)…

Q: Circle the least reactive compound in an SN2 reaction. Explain your choice. H H. CH2I CH,CH,I

A: "Since you have asked multiple question, we will solve the first question for you. If youwant any…

Q: A B гон NO2 но D

A: Hello. Since your question has multiple sub-parts, we will solve the first three sub-parts for you.…

Q: in each structure circle the most likely site of EAS reaction 6. In each structure, circle the most…

A: EAS reaction means Electrophilic Aromatic Substitution reaction where the hydrogen atom of the…

Q: Which SN1 reaction is each pair is faster? А. CI OH2 H20 .CI OH2 H20 CI В. H20 CI OH2 H20 OH2 B,

A: Unimolecular nucleophilic substitution reaction (SN1): This reaction proceeds into two steps. The…

Q: TM H Show the synthetic sequence that converts acetylene to the target molecule (TM) shown below.

A:

Q: エース z-z L H H + CH Anything you need け。

A: Detail mechanistic pathway is given below

Q: Draw the major E2 elimination products from each of the attached alkyl halides.

A: E2 elimination stаnds fоr bimоleсulаr eliminаtiоn. The reасtiоn invоlves а оne-steр meсhаnism in…

Q: Draw the major product of the following reaction and enter its InChl code in the space provided.…

A: This is a nitration reaction, in this reaction nitronium ion generated from the nitrating mixture…

Q: Propose a mecahism for the following reaction and include all relevent reagents (you may use any).…

A: This is a multi step synthesis reaction . By using the starting material with various reagents we…

Q: Predict the major product in the following reaction. Be sure to draw it with well-defined…

A: Answer of this question:- In this reaction syn addition of hydrogen  Hence, the product of this…

Q: NBs, hv CClu

A: This is a radical reaction. In the initiation step, NBS reacts with ultraviolet light light to…

Q: CH3 CH3 CH3 CH3 CH3 H3C Y

A: Interpretation -  To complete the mechanism of the reaction starting from the intermediate  X, by…

Q: Propose an efficient synthesis for the ff. transformations: b

A: a) Transformation 1 -

Q: 2. Draw the complete, detailed El mechanism for the following reaction (including including curved…

A: Tertiary alkyl halide gives E1 elimination to form an alkene. The alkyl halide eliminates hydrogen…

Q: Predict the major product in following reaction sequence (sh

A:

Q: For each pair of reactants (A-C) draw all possible E2 products, label each as a mono, di, tri, or…

A: When an alkyl halide reacts with a strong base, the reactants can undergo two mechanisms. The…

Q: Draw a stepwise, detailed mechanism for the attached reaction.

A:

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: Br or Br Br C or CI || CI or CI ||

A:

Q: NaOH N2OCH3 H3CO OCH heat

A: "Since you have asked multiple questions, we will solve the first question for you. If you want any…

Q: draw out a detailed mechanism showing the transformation from stilbene to stilbene dibromide C14H12…

A: The reaction taking place is given as, => C14H12 + 2 HBr + H2O2 -------> C14H12Br2 + 2 H2O

Q: Br

A: Under polar and protic solvent in the presence of weak base E1 elimination is favored. E1…

Q: N. Br2/FeBr3 CO2CH3 SO/H2SO4 HO. CI AICI3 NO2 HNO3/H2SO4 CN

A: Reaction 1 : EAS (Bromine electrophile). Reaction 2 : Sulphonation ( SO3 electrophile). Reaction 3 :…

Q: Draw a detailed mechanism showing the formation of all products, be sure to draw all intermediate…

A: In the organic conversion, suitable reagent converts the reactant into products. Reagents attacks…

Q: Predict the major product in the following reaction. Be sure to draw it with well-defined…

A: Alkanes are less reactive chemically.  In presence of light Freeradical Substitution Reaction…

Q: How do I rank these from best to poorest leaving group? Do I base it in the size of the…

A: We have to rank leaving group tendency :-

Q: Determine the position that is most likely to be the site of an EAS reaction in the compound below:…

A: The compound given is,

Q: terminal alkene

A:

Q: What is the most likely product from the following sequence

A: The first step of the reaction is the Friedel-Kraft acylation reaction and the second step of the…

Q: Predict the major product for each reaction:

A: At first alkene being nucleophilic undergo protonation to give most stable tertiary carbocation.…

Q: then

A: