H,C..CH, CH, NH CH, CH CI CH, 1. Na,co, NaOH HCI 2. NANO, HCI NaOH draw the reaction mechanism of this synthesis of an azo dye rxn

Q: 8. Give the mechanism of the following reaction: CH,Br + CH,OH → CH,OCH; + HBr

A: Primary halide undergoes SN2 reaction mechanism.

Q: Analyze this reaction mechanism and identify all species that act as nucleophiles in this process: B…

A:

Q: NaOH of CH3 H20

A: Ester is hydrolyzed in the presence of a base or an acid catalyst. In the presence of a base…

Q: Physical Chemistry Q1) In this reaction CH;COOCH, + H,0 –→ CH,COOH + CH,OH Note that the rate and…

A:

Q: Give the mechanism of the following reaction: CH;Br + CH;OH → CH,OCH3 HBr

A: the mechanism is as follows:

Q: Complete the reaction with rational reaction mechanism. CO,H Me =Li cat. H2SO4 H,SO4 HCO,H 90 oč…

A: We have to provide the complete mechanism for the following given reaction as follows in step 2:We…

Q: Na, ELOH NH:(),Et,0 Br2 MeC(O)OOH Et20,-78°C DCM,15°C NaOMe Et,0 Reflux Complete the reaction…

A: Step 1: Birch reduction. Step 2: epoxidation using peracetic acid. Step 3: bromination of olefins.…

Q: Please show complete mechanism with all steps with naming Он OH H2, Pd/C 'N' он МеОн, EtOH 23 °C,…

A: Note : Deprotection of benzyl using H2 and Pd-C. This reaction is called hydrogenation. Using…

Q: Draw curved arrows to show the movement of electrons in this step of the reaction mechanism.

A: To draw the curve arrow mechanism for the following reactions.

Q: 2. The following chemical transformations involve multistep mechanisms. Please reasonable mechanism…

A:

Q: 1) NaOCH3 H3CO OCH3 2) H+

A: Dieckmann condensation is the intramolecular chemical reaction between diesters that gives beta keto…

Q: он МСРВА CH;Cl, но HO

A: In step 1, first there is a nucleophilic attack of lone pairs of oxygen resulting into formation…

Q: NCO

A: Given reaction,

Q: H,SO4 Cl, H,SO, (conc.) FeCl, (dilute)

A: 1) Toluene reacts with conc. H2SO4 is sulphonation reaction  2) second reaction is chlorination  3)…

Q: Show all of the steps in the mechanism for this reaction: CH3 CH3 CH;-C-CI CH;OH CH —С—ОСН, + HCI…

A:

Q: OMe OHC, KOH/ N OMe ÓMe OMe OMe ÓMe

A: Nucleophilic addition reaction: Addition reaction in which an nucleophile is added to electrophilic…

Q: NaNH, NH3 (-NaCi) NH2

A: Benzyne is a reaction intermediate. In order to generate benzyne, sodamide in ammonia is used. The…

Q: Draw the complete mechanism for the reaction below. Sheet. Br Br2 hv

A: The addition of Bromine with allylic alkenes is proceed by Free radical mechanism , it is known as…

Q: OMe cm Clz mCP BA MeO `OH

A: Given reaction is example of Baeyer-Villiger oxidation. The Baeyer–Villiger oxidation is an organic…

Q: OH OH ∞∞ BF3 Et₂O This reaction takes place via a pinacol rerrangement. Please, draw curved arrows…

A:

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: Give a complete mechanism for the intramolecular reaction below. You can leave the reaction…

A: Alkenes in presence of Br2 give disubstituted bromine product. The reaction proceeds via a cyclic…

Q: Show the reaction mechanism for the acid-catalyzed hydrolysis of methyl ethanoate. Clearly show all…

A: The acid catalyzed hydrolysis of methyl ethanoate results in the formation of methanol and methanoic…

Q: What is most likely the first step of this reaction's mechanism? CH CH;CH,OH Br Br CH;CH20- -- CH3…

A: Interpretation-  To tell about which one is the most likely the first step of this reaction…

Q: HO H. H. NH OH HNO3 N. H,SO, HO HNO3 N. CH3 H,SO4

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

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

A:

Q: CH,N2 CH,N2 H,C-NEN HO,

A: Carboxylic acids reacts with the CH2N2 reagent to produce esters.

Q: MeO CH;CH,NH2 CH,OH + O=

A: Given reaction,

Q: 1) ВН-THF 2) H-0г. NaOH 3) РСС, СH-Cla

A:

Q: Catelyst Rucly CPPh37, me

A:

Q: What will be the dominant mechanism that occurs in this reaction?

A: 6- E1 mechanism is a two step mechanism whereas E2 is a one step mechanism

Q: PPH3/CBr4 PPH3 Br HOʻ PPH3

A: Welcome to bartleby !

Q: Q2. Show the mechanism of the following reactions. N3 THF, rt `Br + NaNg reflux i. + CH;OH a ii.…

A: i) Axial attack of N3- is favored  ii) The reaction undergo SN1 mechanism. iii) The reaction…

Q: 15 EtgSiOTf (16) CH;CN OTf EtO EtO Show the mechanism for this reaction

A:

Q: Q1) In this reaction CH,COOCH, + H,0 –CH,COOH + CH,OH Note that the rate and order of the rection…

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

Q: How many steps in the mechanism of this reaction?

A: Number of steps in the mechanism of given reaction = ?

Q: .ce AICly

A: This is the friedelcraft reaction .

Q: H-N CCH3)2 CH3 CH3 H304 CH3 CH3

A: Applying concept of addition elimination reaction.

Q: N H .N. NaNH2 CI CI

A:

Q: Draw a reasonable mechanism for this reaction. Interactive 3D display mode Ph Ph-P=CH, CH2 Ph

A:

Q: CH,CH,СH, CI CH,СНHCICH, + 2HCI 2CH,CH,СH, + 2C1, The chlorination of propane proceeds as a radical…

A: A chemical reaction is symbolic representation of the conversion of substances to new substances.In…

Q: Give the complete mechanism for the following reaction: CH3CH3 + Cl2 CH3CH2CI + HCI ----

A:

Q: D. Provide a reasonable mechanism for the following reaction. ·CCL 3 1. NaOH, H₂O 2.H₂O* он

A:

Q: HCO2ET, NaOMe ? RT, 30 min 94 % H.

A: 1. NaOMe abstract the acidic proton that is alpha to carbonyl group. 2. Product is addition of…

Q: Br 1) NACN, DMSO 2) excess LAH 3) H20

A: Organic reaction mechanisms:

Q: OH -NO

A: The question is based on the concepts of Organic reactions. we have been provided reactant.  we have…

Q: LIAIH4, THF, 0 °C, но 45 min, 73% Me Bn Me 6 7

A: This is the deprotection of chiral auxiliary by LiAlH4.

Q: d) Write a mechanism for this reaction: AICI3 HCI + CH,Cl, CI

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