CH3OH (-HCI) CI ???

Q: then Br then Br Br

A: Solution: We know alpha hydrogen to the any carbonyl group are acidic. If there are two different…

Q: The reaction of 3-methylpent-2-ene A with HCl can lead to two possible regioisomeric products, B and…

A: The solution of the question is given below:

Q: In the proton transfer step of a Friedel-Crafts alkylation reaction, where does the proton go? O To…

A: Given  proton transfer step of Friedel-crafts alkylation  To be determined  Where does the proton go…

Q: 4. Write mechanism for the reaction and predict the final product. CHO CF3COOO

A: Benzaldehyde on treatment with trifluoro peracetate produces phenyl formate. This reaction is an…

Q: Name the PRODUCT compound and give it's molecular weight Q. Which is a better nucleophile methoxide…

A: Nucleophile takes a negative charge or lone pair of electrons on itself and attacks on a positively…

Q: What are the groups towards meta position give examples and what its mechanism ?

A: The meta-directing group generally are the electron withdrawing group that direct the upcoming group…

Q: C/

A: Elimination reaction is the reaction in which small molecules like water and ammonia is eliminated.…

Q: Using curved arrow formalism, give the mechanism for the following reaction. Be sure to include…

A: Given,

Q: Give a detailed explanation on the reaction of tje compound and its mechanism and why did it happen.…

A: Explanation for the reaction of butanol with HBr.

Q: heel HO он NaOH (a)

A:

Q: Write the complete stepwise mechanism of the following reaction. Show all electron flow with arrows…

A:

Q: Problem attached

A: The organic reactions are carried out with the help of specific reagents. Every reaction is guided…

Q: Complete the diagram by drawing the structures of B and C for this mechanism: H* B do

A: Given,

Q: CrO3, H2SO4 acetone

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

Q: Predict the predicted product of the reaction shown in the following diagram:

A: -NH2 group is strong ring aactivation group, hence when amino benzene (aniline) is treated with…

Q: TsO, Et,N: DMSO

A: Removal of OTs gives a carbocation which undergoes ring expansion via alkyl shift to produce another…

Q: Illustrate the mechanism of forming alkynes from a 1,2-dihalide and a vinyli halide. Show…

A:

Q: CH,CH-CH: 1. CH, CHLOO OCH CH₂ 2. HCI

A:

Q: III. Give a detailed mechanism for the following reaction: HO, CI

A: Given reaction: We have to write the mechanism of the reaction.

Q: OTs - (strong base) В Doubling [B] doubles rate of rxn.

A: The reaction involves a carbocation intermediate and is commonly seen in reactions of secondary or…

Q: Provide a reasonable mechanism that provides the major product for the reaction scheme provided…

A: The reaction given is,

Q: a) ОН ОН b) CI HO

A: Here we have to prepare the following compounds from the given starting material in multistep…

Q: Give any reaction to show asymmetric synthesis.

A: Asymmetric synthesis. A  particular synthesis where a new chiral centre is created in an optically…

Q: Show a mechanism for how the product is formed. Your mechanism must use curved arrows to represent…

A: Given : reaction It is an elimination reaction, since strong base is given so it is E2 elimination.

Q: HiCan you help me with this question?

A: Secondary or tertiary alcohols reacts with Lucas reagent (HCl and ZnCl2) by SN1 mechanism and forms…

Q: Explain and provide the mechanism of the reaction. Name the final product with the assignment of…

A: The mechanism for given reaction is shown below,

Q: H OH + H-CI = `CH, CH,

A:

Q: show the formation of the nitronium.

A:

Q: + H;O+ HO

A:

Q: hv . 3D

A:

Q: Br2 NEIS A CH,Cl2 CH,BrO;

A: Reaction 1 : Bromine addition to olefin. Reaction 2 : E2 elimination.

Q: Give the complete, detailed mechanism for the following reaction. Be sure to include an explanation…

A: Given reaction,

Q: Give the detailed mechanism for the following nitration reaction. Show the contributing resonance…

A: To solve this problem we will write the mechanism of the given reaction .

Q: for the Cl2 addition reaction with 1,2dimethylcyclohexene, draw the most reasonable curved arrow…

A: Cl2 when reacted with alkenes, add to opposite faces of the double bond, that is in an anti-addition…

Q: Use the step-wise mechanism to predict the final product of the reaction below. SOCI, он

A: Since you have posted multiple questions as per guidelines we can solve only one per session . If…

Q: A student found that heating any one of the isomers shown here resulted in scrambling of the…

A: Given, Here the compound undergoes a 1,5-hydrogen shift of D or a 1,5-hydrogen shift of H. in each…

Q: Predict the product of the following reaction (support your answer with the mechanism):

A: This is is grignard reaction.  Grignard reagent is organomagnesium halide which contain…

Q: Write o o mechanism to hronsform Compound A to B NH2

A: For reaction 1, we will use aniline (which is used as polymer)  For reaction 2 and 3, we will use…

Q: Provide the reaction (reactants -> products) with detailed mechanism for the following, with AICI3…

A: Given: Reactants Toluene + CHCl3Benzene + CHCl31-Hexene + CHCl33-Hexene + CHCl3 To find: Detailed…

Q: A B но NCI Í + N-O C

A:

Q: Provide the major organic product in the reaction below. CH,CH2 + NaOCH, CH

A:

Q: O Complete the following reaction and provide a detailed, step-by-step mechanism for the process.…

A:

Q: (b) Complete the following reactions and suggest plausible mechanism. Mention the step where the…

A: The Answer Of the Following Questions are given as below:-

Q: Ach 1LAIMY pels

A: Since you have asked a question with multiple sub-parts, we will solve first three sub-parts for…

Q: H2Oz, HO-S-CT, Ho- (Re

A: The mechanism of the above organic transformation is given below

Q: 1) NaOH H 2) H*, heat

A:

Q: the mechanism of halogenation of thiophene, when the halogen added to the position 2 and 3 , also…

A: Thiophene is an electron rich hetrocyclic compound. The resonating structures of the thiophene will…

Q: Study the curved arrows in the reaction and provide the line structures of all the intermediates and…

A:

Aldehydes and Ketones

Aldehydes and ketones are organic compounds that have a carbonyl group, C = O, as their functional group. They both differ in the placement of this carbonyl group in their structures.