In 4 sentences or less, explain why the reaction below only occurs under thermal conditions. hv A Enter your answer here

Q: Predict the main product of the reaction in Figure 10.

A: Alkyl bromide reacts with ammonia, a nucleophile to give a nucleophilic substitution reaction to…

Q: b) What is the heat of reaction for the overall equation? Show your work. c) Which step is the rate…

A:

Q: H HO, AICI3 H HO HO. HO HO A B D

A: It is friedel craft alkylation reaction. -OH group is ortho para directing group  -CHO is meta…

Q: . Carry out following conversion. Provide suitable reagents, reaction conditions and also…

A:

Q: Which of these would be the fastest to react via Sy1? .CI A) B) CI CI C) D)

A: SN1 is also called unimolecular nucleophilic substitution reaction.

Q: OH

A: 1. This reaction is in thermodynamic equilibrium state.  2. Here products and reactants are in…

Q: Provide a plausible arrow pushing mechanism for the reaction below. cat. TSOH, A + H20

A: acidic Aldol mechanism  with full arrow steps involved in step-2

Q: H. NH2

A: The reaction taking place is given as,

Q: Show the mechanism and the final product of the reaction shown below: H O OMe MeO H2SO, N. NH2 ZIR

A:

Q: H+ SOCI2 NH3 CH3 ?

A:

Q: Write a mechanism for this reaction: d Alld Both others o beyond Labr, all rights reserved Para bmes

A: Step wise reaction mechanism for friedal crafts acylation is explained below.

Q: 2) Justify why this reactions did not work SMe2 Conjugate addition H2Cr2O7 Oxidation

A:

Q: What are the major products of these reactions (pls show the mechanism so i can understand how to do…

A: Hello. Since the question contains multiple subparts the first three subparts are solved. In case…

Q: Provide

A: Tertiary alkyl halide in polar protic solvent undergoes alkene.

Q: Could the reactions shown here take place by a concerted mechanism?

A: A concerted mechanism can be drawn as

Q: Br HBr

A: available lone pair on O-atom acts as lewis base, H+ acts as lewis acid and lewis acid-base reaction…

Q: Please solve for the following Stretter Reaction showing the steps and the final product.

A:

Q: Do the reactions below proceed in good yield from left to right as shown?

A:

Q: Describe three ways the following reaction can be carried out:

A:

Q: For the following reaction, draw the correct product that you would expect to form under Robinson…

A: Given - Product = ?

Q: For each reaction, I need to make bromination (Br2) and show reaction mechanisms: Initiation;…

A: Free Radical Reaction  Bromination of 2 degree aliphatic and 3 degree aliphatic compound

Q: Please show the complete steps as well as arrowing pushing mechanisms for the following reaction.

A:

Q: Fill in the box with the major organic product of the following reaction mechanism. NaOH Draw the…

A: -> Base can abstract most acidic proton from the compound . -> In case of alcohol proton…

Q: Please solve for the following reactions and show all arrowing pushing steps.

A: The details mechanism for the reaction is provided below in attach image.

Q: What alkyl halide product (from Figure #10) results from the following reaction (from Reaction #10)?…

A: In the given reaction ether reacts with hydrogen bromide to form alkyl bromides. The reaction…

Q: Analyze the reaction below, and determine the reagents necessary to carry out the conversion. Be…

A:

Q: Which solvent listed below will result in the highest rate of this reaction?

A: Given reactant  is 3° butyl chloride hence it undergo through SN1 mechanism.  In SN1 mechanism…

Q: CrO3, H2SO4 acetone

A: CrO3.H2SO4 also known as Jones reagent which is used for oxidation .It oxidizes primary alcohols to…

Q: How is this incorrect and what is the correct mechanism?

A: Given : We have to tell what will be the correct mechanism.

Q: Show the mechanism for the reaction conducted at-5 "C in CCI,. cyclohexene + bromine…

A: Given reaction is addition reaction.

Q: kindly answer a and b, asap. Thank you!

A: The structure of the given compound is :

Q: In 4 sentences or less, explain why the reaction below only occurs under thermal conditions. hv

A:

Q: Please help me this question! Thank you! Show the mechanisms of the reactions below

A:

Q: HO: What is wrong with the mechanism described below?

A:

Q: Describe two ways the following reaction can be carried out

A: Wolff Kishner reduction is a reaction to reduce ketones to alkanes. The reagent used to reduce…

Q: Provide a mechanism for the reaction below: H H. HCI

A: Chloromethylation is reaction of aromatic rings with formaldehyde and hydrogen chloride. The…

Q: show me and explain the mechanism for this reaction please

A: In the above reaction, since the alcohol is 2 degree, hence the reaction is happening  The above…

Q: 2. Answer ALL parts. a) Write a detailed reaction mechanism for the following conversion. он Acetone…

A: Here we have write the reaction mechanism of following given conversion.

Q: from b.

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

Q: HONH, CI- , NaOH

A: This is an example of condensation reaction in which hydroxylamine condensed with 1,3-dikketone to…

Q: Could the reactions shown here take place by a concerted mechanism?

A:

Q: Provide one example for E2 reaction of alkyl halide

A:

Q: pts) Show any reaction that would involve the rearrangement of an intermediate carbocation.

A:

Q: H20/H*

A: The answer of this question given below

Q: H. ? H,O H. ether NaBH, THF ?

A:

Q: 2. Answer ALL parts. a) Write a detailed reaction mechanism for the following conversion. ОН HO…

A: We have to give the mechanism of the given reaction.

Q: a) Show a detailed mechanism for the reaction to produce nitrogen gas and the two carbon radicals…

A: "Since there are multiple sub-parts in this question and it is not mentioned that which one has to…

Q: Please help, need to figure out the mechanism for the starting group (the first one)

A: Here we have to synthesize the following given target compound from starting material benzene and…

Q: HO.

A:

Q: Please complete the reactions given below.

A: Given reactions: g)                               h)                                i)…