Drawa mechanis m for this reaction, Dredictiny the Droduct -Be Sure to label eacharrcw withits Datterrn And show Stereochem is try explicitly :Br: + Na:=N:

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A: Rules for elimination: Proton trans to the leaving group (Br in this case) eliminates Br should be…

Q: Draw the MAJOR products A - E for the following reactions. i. KMNO4, HO", heat SOCI, A В ii. H;O" i.…

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Q: d) H+ NaOCH, носн, носн,

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Q: H,SO,. H,0 2. Zn, H,O* 1. O, Brz, CH,OH KMNO,, H,O* 1. BH, 2. NaOH, H,O,

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Q: Draw a mechanis m for this reaction, Dredictne the Droduct -Be sure tolabel eachanraw with its…

A: The given reaction follows SN2 pathway as shown below -

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A: We will give products of all reaction

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A: In this question we have to synthesis the compound X and also write its mechanism.

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A: Alkene on hydrobromination reaction forms alkyl bromide.

Q: Drawa mechanis m for this reaction, Predic the Droduct tory -Be sue to label each anrcw with its…

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Q: woite the major products with relevant stereochemitry. Ques 12o°c a) NHTS b) (CH,0), 50,, benzune…

A: Solution: the major product with relevant stereochemistry is drawn below

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Q: For each of the tolowing reactions predict the major product. NaOH H,0, A Raney N. A préssure OH…

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A: Organic reactions: Detailed mechanism and explanations are given in the following steps

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A: Since we know that in E2 elimination reaction Proton and leaving group should be antiperiplanar...

Q: Which isomer of 1-bromo-2-tert-butylcyclohexane reacts faster when refluxed with potassium…

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Q: Qj writhe produebs obtained byozoholysi of Tue follbwing Compounel I 12 dimethgl-l-octene 1,1…

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Q: 1. Draw the MAJOR products A - E for the following reactions. i. KMNO4, HO", heat SOCI, A В ii. H;O°…

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Q: Draw the product of the following reaction, including stereochemistry. H OTs Na* "OCH,CH3

A: When compound OTs are treated with base NaOCH2CH3 then elimination reaction occur.  The reaction…

Q: Deaw the peoducto of Jequences ohawn belw. Ignore inorganic bproducts. tuwo Step Leaction 1. NacN 2.…

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Q: Meo. Mea * IS Bthe thermodynamic ol kinetLC product? Meo → Meo k design a syntnesis to convert B to…

A: The solution is as follows:

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Q: NaBr Mechanism(s) e) (Hint: is this reaction stereospecific or stereoselective?) Br NaOH…

A: Substitution reaction is type of organic reaction where one functional group is replaced by another…

Q: NaH (A) CH,-(CH),I PI HBr (excess) OH NaOH МСРВА (B) CH;Cl, PII H,SO, MeOH EtOH PIV PIII…

A: PI : There are two products formed. Since the HBr is in excess amount so it will lead to alkyl…

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A: This is an example of Diels-Alder reaction

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Q: by Eg-eliminedion Q: What is favorable Product Reaction. PPha H. Ea Me n.

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Q: draw a structural formula for the more stable carbocation intermediate formed in the reaction shown

A: In the following reaction, two carbocation intermediates can be formed.

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A: The  reaction is :-    We have to find out the product of the above reactionThis is simple addition…

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Q: Provide the missing major product, reactant, or reagent and the mechanism (e.g. SN1 or SN for each…

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Q: NaBH4 OH OH LIAIH4 OH H. I OEt H. chemoselectivity How an do this reaction?

A: ->NaBH4 can not reduce ester group. ->LiAlH4 can reduce both ketone and ester into alcohol.

Q: 4. Prodiet the productis) of the lollowing reactions, including stercochemistry when necessury und…

A: Nucleophilic substitution reaction

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A: To find: product formed by the following reaction:

Q: Itis Known that at 120°c k = 10ms %3D -7 At 27°c Fz= 10'st Eace) = 80 kcal mot Deterrmine the…

A: As we know, for parallel reaction, we have following equations: [B]=-k1[A∘](k1+k2)e-…

Q: comprunds Y yhore th Compound X has paden uinonte , A= 271 (s) 8- 2-19 L) ond lompeund y has A= 2-77…

A: This problem is based on nmr spectroscopy