i. El or E2? | i. Rule? iii. Arrow-pushing Mechanism & Major Product Br NaOEt 'Br KOC(CH3)3

Q: )CHz MgBY 2) AQ. Workup 3) PBY3 -CH3 Br

A:

Q: H₂C. a) Propose initiation and propagation steps (termination is not required) to explain the…

A: Initiation is the formation of first radical

Q: Show the mechanism using curved arrows.

A: The mechanism for the give reaction can be shown below

Q: Use full-headed or half-headed curved arrows to show the movement ofelectrons in attached reaction.

A: The given chemical reaction is represented as follows:

Q: Show Steps for Mechanism and Box Final Product D HBr, ROOR La) 2 PP hg 3) Buli 4) (CHg)z C =0 ) Mg,…

A:

Q: Please draw chemsketch of this by using any software like kingdraw or chem draw. And send this…

A:

Q: Show all working explaining detailly each step Answer Q2a(i), (ii) (iii) and (iv)

A: Without catalyst reaction have to break the highest energy barrier. Catalyst decrease activation…

Q: Which scheme shows the correct arrow pushing mechanism? Br scheme 1 scheme 2 H? Br > scheme 3 scheme…

A:

Q: H. NH2

A: The reaction taking place is given as,

Q: OTs HO 2)

A:

Q: pyridine OCH3 NH2 ÓCH3 FmocCI

A: Fmoc-Cl stands for 9-fluorenylmethyloxycarbonyl chloride. The structure of Fmoc-Cl is represented as…

Q: NO2 CI

A:

Q: Do all that's asked please label so I know

A: The question is based on molecular properties of the compounds. Lewis structure is a method of…

Q: Br NaOCH3

A:

Q: (c) OH H* ?

A:

Q: Cutline an electron pushing mechanem (mechanem ghould ncccunt for any Storebchomical and…

A: Amines are the compounds containing the functional group of R-NH2. Carbonyl compounds are the…

Q: Step 3: add curved arrows. Step 1: add curved arrows. Step 2: add curved arrows. Select Draw Rings…

A:

Q: Br. SO3H

A: Ans  Electrophilic substitution reaction initially sulphonation then bromination of benzene

Q: Draw the isolated pentadiene

A: We have to draw the isolated pentadiene .

Q: Indicate the predominant mechanism: Sn1, Sn2, E1, or E2.

A:

Q: i Provide the missing curved arrow notation for the E1 mechanism.

A: In the E1 mechanism which is also known as unimolecular elimination, there are usually two steps…

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

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

Q: please

A: Triphenyl phosphine act as Nucleophile because it contain lone pair on phosphorous atom so that it…

Q: CH3 + НаС — сн н

A: We have to predict the mechanism for formation of given product via Michael addition.

Q: Add curved arrows to the structures shown below in order to complete the mechanism. OCH3 OCH3 НА OH…

A:

Q: Br t - DuOK Me DM SO

A: The base will abstract the proton and causes ring opening.

Q: Show an exampIe for intramoIecuIar cIaisen, mixed aIdoI and conjugate addition including a full…

A: Intramolecular clasien Condensation :

Q: НО NaOH (CH3),N (CH3),NCH,CH,CI Can you show this mechanism please?

A: Nucleophilic substitution biomolecular reaction (SN2): The bimolecular nucleophilic substitution…

Q: NBs, hv CClu

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

Q: Can you show the mechanism and the products for those problems especially the ones that I put circle…

A: Benzene shows aromatic electrophilic substitution reactions because it does not loose the…

Q: NBS DMSO, H2O

A: In the reaction between alkene and NBS in water, the anti addition (because the water will attack…

Q: Show all working explaining detailly each step. Answwer Qb(i) $ (ii)

A:

Q: Step 1: add curved arrows. Step 2: complete the structure and add a curve arrow. Draw only one…

A: The given mechanism is hydrolysis of ester to give carboxylic acid and alcohol.

Q: mechanism for this “Cannizzaro reaction”

A:

Q: prourde reagent tocary followng vans tormation. out the

A: Solution: Due to carbonyl carbon of ester it shows nucleophilic substitution reaction. This is the…

Q: please

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

Q: + HA Please write the mechanism arrows for it as an Sn1 mechanism please

A:

Q: mechanism? Explain why. Explain why this reaction gives more inversion than retention of…

A: SN2 will give an inversion of configuration and SN1 will give a racemic mixture. SN2 works for…

Q: Br OH NaH CH3I DBU DMSO H2/Pt

A: In this reaction,  Given different reagent , using this make the product, these reaction.…

Q: CH3

A:

Q: This molecule undergoes an E1 mech. 1st attempt Add the missing curved arr

A: Alkyl halides undergo elimination and nucleophilic substitution reactions. Elimination reactions are…

Q: Add curved arrow(s) to complete step 2 of the mechanism. ---- CH3 ÇH,

A: The step of the mechanism given is,

Q: RX AIX3 'R H2. Pd AIX3 ELOH Noem een nadeel van elke reaksie. Name one disadvantage for each…

A: 1st reaction is friedal crafts alkylation. Major Disadvantage of this reaction is: The halide must…

Q: CH но- H,C Apply Mechanism :OH Hint Solution 8 remaining step(s) can be solved Tip: Only add curved…

A: In the given reaction the carboxylic acid reacts with sulfuric acid. The main role of the acid…

Q: show mechanism please using s like Sn1 Sn2 E1 E2 رے سلHo Но

A:

Q: Two propagation steps are given. Select the appropriate curved arrows for bond making or breaking by…

A: The appropriate curved arrows for the above propagation step is given to

Q: 3) N Br ->

A:

Q: 11. heat -N+-CH3 CH3 12. 1) NaOCH3 H3CO OCH3 2) H*

A:

Q: Find major product of this - show reaction mechanism and all selectivity. а.) Brz hy b.) Rha COAC)4…

A: Let us solve these reactions.