Cutline an electron pushing mechanem (mechanem ghould ncccunt for any Storebchomical and reaiochemical adcome)

Q: Hou could the fallowing frmsformatione take Place ? Please show complete mechanism pd proper…

A: Nucleophiles are nucleus loving species and electrophiles are electron loving species. The strong…

Q: acture of the major organic pr«

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Q: OR A ZI

A: We have to choose which one is more basic.

Q: hat is the orientation (syn or anti) of the compound?

A: When two compounds has same molecular formula, but different arrangement of atoms in space,such…

Q: of a ne c

A: We know that, the EMF of Westron standard cell is 1.0153 at 20∘C.

Q: fallowing What are theproducts reactions. Draw mechanis.m. and specify their stereachemistry- fthe…

A: since you have posted multiple questions in a single session, we are entitiled to answer only first…

Q: (a) How can you tell that the wmpound cinled in puuple is Zait ev broduct, whereas the umpouhd ok…

A: Zaitsev and Hoffman's  product : Zaitsev is the product where the double bond is  more alkylated or…

Q: fre a) which is the most

A: According to the question, we have four free energy/reaction diagram.   (a) For an exergonic…

Q: What is the orientation (syn or anti) of the compound?

A: When two atoms are added to the unsaturated bond on the same side it is said to be a syn…

Q: OTs HO 2)

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Q: Leite product and meehaniun PAGE NO. DATE:

A: Hoffmann bromide reaction is a type of reaction used for the conversion of amide to amine. This…

Q: regiochemistry and/or configuration

A: The given blank has to be filled correct regiochemistry and/or configuration

Q: Draw all eson ance for nitrile imne

A: Given is the structure of nitrile imine Here we are required to draw the resonating structure of the…

Q: Using the reagent sheet, identify the reagent needed to carry out the transformat OH IReagent)

A: Applying concept of halogenation, elimination, ozonolysis and oxidation reactions.

Q: Noting the curved anows, draw all the product(s), organic and inorganic, of the following reaction.…

A: The curved arrow shows the movement of electrons. The electrons are move from the nucleophile to the…

Q: en deciding between 1,2-addition, 1,4-addition and the major reaction pathway, there's ually an…

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Q: CH, + H,C CH3CH2CH2OH ČH,

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Q: your performed a Ad extraction Iquid-liquid to isolate isopentyl acetate every the isopentyl acetate…

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Q: n two of uiese Teaction sequences will this transformation?

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Q: rganize the following me

A: The oxidizing agent is that reagent that reduces itself but oxidized others. The can gain electron…

Q: Circle one or more: SN1 SN2 E1 E2 OMs NaSPh, THF Mechanism:

A: Given reaction:

Q: Wite out He steps necessany To make CH3CHZ! Starting with ettyne end any Other Chemicab.

A: The answer is given as follows

Q: How Can Synthy's! Ep the compound pleas start whith simple and Commercial available Startuy materia)

A: This Reaction is done via Aldol condensation.

Q: а. arbousto CH3 abnuoginod. С. b.

A: Rule of IUPAC- 1) Longest chain as parent chain. 2) Numbering start from those side where more prior…

Q: Plz do Asap...! With proper reaction with mechanism...!

A: The above reaction is Benzonitrile to Acetophenone. Benzonitrile is first treated with Grignard…

Q: conditichs Reachion takes place unoleracidic Led Pronde an amow mechanism N HL O meehanum Kor…

A: This is known as Mannich reaction.It undergoes via the formation of Mannich base.

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

A: Intramolecular clasien Condensation :

Q: Draw a meso compound for the attached molecules.

A: Meso compounds are the achiral compounds containing a tetrahedral stereogenic center. The…

Q: SOCL주

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

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Q: In the radical inhibitor mechanism depicted below, when do you put the radicals above the arrow vs.…

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Q: Draw curved arows (mechanism) to show how CH3CH=CHCH3 reacts with HBr to form a carbocation…

A: Addition of HBr to alkene gives the corresponding alkyl halide. The reaction proceeds in the…

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: Noting the curved arrows, draw all the product(s), organic and inorganic, of the following reaction.…

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Q: Eom form a synthetic pathway 6or tanget molecule Stauting mateuials must a maximum of 6 Carbons and…

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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: 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: 1.) Proride a detailed following transformution. Show all maer resonunie For curved arrow mechanism…

A: An organic reaction in which the incoming nucleophile takes the position of a leaving group is…

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

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Q: prounde reagent tocary followngons tormation. out the

A: Answer is explained below.

Q: atleast 1 or 2 answers needed

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Q: S) Prndea nablemechanism for tre reaction Hices?

A: Cleavage of ether in presence of HI.

Q: A detailed mechanism for the trensformation below. ome Has Oy s 1) so°c ome on

A: Since the OH in the reactant is nuclophilic due to presence of lone pair electron. Hence it takes…

Q: 3) N Br ->

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Q: Is the attached specy conjugated ?

A: Conjugation takes place if the double bond/negative charge/positive charge is present alternate to…

Q: Draw the strue fune of he ogmfe major prodvet of the following reachions.?

A: Carbonyl compound (aldehyde and ketone) reacts with an alcohol to form hemiacetal in the presence of…

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

A:

Q: Give a clear handwritten answer....

A: Here we have to synthesise the following given compound from starting material benzamide.

Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.