Predict the product (s) of the following reaction. Show the mechanism. Explain.

Q: dilute HCI

A: The addition of HCl to alkene yield alkyl chloride. The addition process follow Markovnikov rule.…

Q: 2. CH₂CH=CH₂ + HCI HCI →>

A:

Q: (Product) + Soz Mechanism of the reaction

A: The reaction of ethanol with thionyl chloride in the presence of a base like a pyridine will result…

Q: Q Grubbs 2nd Generation Catalyst ethene R

A: Grub's catalyst is the transition metal complex that involves ring closing and ring opening…

Q: OCH3 AICI3

A: The reaction given is,

Q: H2SO4 HO HO

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: Predict the products of the following reactions.

A: For drawing all reactions the molecule indicating as a simplest notation. All the reactions are…

Q: How

A: We will write the mechanism

Q: Hz O heat

A: The given reaction is the nucleophilic substitution reaction. H2O is the nucleophile that will…

Q: Give the major product of the following reaction. MeO H2

A: Given,

Q: give the product (s) of the reaction when it reacts with HBr/ROOR in presence of heat or energy.…

A:

Q: LOPH N° NaH Но. Ме Phi `CI 1% Ir{dF(CF3)ppy}2(dtbbpy)PF6 3% Cu(OTf)2 7.5% 1,10-phenanthroline blue…

A:

Q: NaOBut CH NO, 2.

A: This reaction is Condensation Reaction because nitro Compound Condensed with alpha-beta unsaturated…

Q: HO + H2SO4, heat – major + minor products OH РСС

A: 2-methylbutan-1-ol on heating with sulfuric acid forms 2-methylbut-2-ene as major product and…

Q: CH3 CH3 CH3 H3C-Ċ-CI CH3 ČH3 + HC1 AICI3

A:

Q: Ts H,C- S-CI ÓH only geometric isomer OO, (тCРВA) OCH,CH, i) NaH CH,0 CH,0 racemic racemic two…

A: Tosylation of alcohol by tosyl chloride in the presence of pyridine gives corresponding tosylated…

Q: light Br2, k ROOR HBr но н soch pyridine

A: as per the honor code we are bounded to solve only first three sub parts. for other sub parts please…

Q: 1 mole of NaCN Br CI DMSO ÇI NaSH acetone H3C `CH3 2-bromobutane + Mg (in anhydrous ether) →

A: NaCN acts as a nucleophile in which CN- is a group that attacks at the nucleophilic centre of the…

Q: a) Brz, light b) ROOR HBr

A:

Q: please help show the mechanisms.

A: Conjugate addition of nucleophile to the unsaturated carbonyl compounds is known as Michael…

Q: + H I + H H-O- -H I

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: + Nal + NaCl

A:

Q: from

A:

Q: Chapter 11 Br B 1) NaNE₂ 2) H2O 3) CH3Cнген Br 4) Na, NH₂

A: Please find the attachment.

Q: Give one example of elimination reaction (E2) type. Show the reactants materials and the product.…

A:

Q: Meo Rh ,(mandelate), (4 mol%) CO,Me CO,Me DCM, reflux, 10 min then add DBU, 2 min; OR Meo OMe OR MeO…

A: Step 1: carbene reaction with double bond generates a cyclopropane ring. Step 2: Under thermal…

Q: a) H20 ? b) Br2/H20 ?

A: The question is based on the concepts of Organic reactions. These involves reaction of alkyl halide…

Q: Please give me the reagents and show the mechanism. Thank you so much.

A: These reaction involes the Michael addition reaction. Michael addition reaction involves the…

Q: Provide the final product and mechanism for the following reactions

A: All the explanation is given below -Explanation:

Q: CH3 H-Br Br он 65 °C CH3

A:

Q: H;O*

A: In the given reaction the alkene is hydrated to form an alcohol.

Q: Br OH 1. NaH 2. 3. H30+ HBr PC13

A:

Reactions at the Alpha Carbon Atom

The position next to the ketone or aldehyde functional group is termed as alpha position and the reaction which occurs at alpha position is called alpha substitution reaction. In an alpha substitution reaction, the alpha proton atom is substituted by an electrophile by the formation of an enol intermediate or enolate ion intermediate. Most of the carbonyl compounds go through an alpha substitution reaction.