24. For the following acid-base reaction draw the correct curved arrow mechanism; CH3-CH2-CH2-CH-SH + OH -----> CH3-CH2-CH2-CH-S +H2O

Q: Complete the mechanism for the reaction of butanone with NaBH, followed by the addition of aqueous…

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Q: Draw curved arrows to illustrate the mechanism for the reaction of 3-methylbutan-1-ol and HBr. The…

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Q: X Complete the following reaction 0/3 O CH3CHCICH2COCH3, AICI3 О снзсн2сH2сосі, AICI3 CH3CHCICH2CH3,…

A: Freidal crafts reaction

Q: 10. Draw a reasonable mechanism for the following reaction (cat. = catalytic %3D amount). OH H2SO4…

A: Rearrangement of carbocations.

Q: Add curved arrows to draw the first part of the mechanism: tautomerization of a ketone to an enol.…

A: Keto-enol is a type of structural isomerism which involves a keto form (containing C=O) with alpha…

Q: Complete the mechanism for the reaction of butanone with NABH, followed by the addition of aqueous…

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Q: appropriate H3C CH3 Br КО-+-Bu ID НО-+-Bu a. CH3 NaOEt b. Ph-c -Br CH3 c. Show the curved arrow…

A: In the two reaction, the first one is an elimination reaction. Second one is nucleophilic…

Q: 4. Draw mechanisms for the following reaction (or sequence of reactions): HO.

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Q: Consider the following reaction. cat. ACOH el H2N-NH2 Toluene (reflux, remove H2O) a. Draw a…

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Q: Draw a complete mechanism for the following reaction. Be sure to start with the formation of the…

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Q: Draw the major E2 elimination product from the following alkyl halide. CH(CH2 HO CH, a draw…

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Q: Draw the Mechanism of Ether Cleavage in Strong Acid—(CH3)3COCH3 + HI → (CH3)3CI + CH3I + H2O

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Q: Draw a detailed mechanism for the bromination of benzene

A: The general reaction is as follows, The mechanism is as follows, First, the Lewis acid-base…

Q: Add curved arrows to draw the second part of the mechanism: tautomerization of an enol to a ketone.…

A: Given the first step of this reaction is the electrophilic addition of deuterium (D).  Second step…

Q: 5. Draw a detailed arrow pushing mechanism for the following reaction. Is the rate-determining step…

A: When No carbocation is formed then reaction is SN2.if carbocation is formed then reaction is SN1

Q: Draw the major organic product of the reaction. Indicate the stereochemistry via wedge-and-dash…

A: • Nucleophillic substitution SN2 reaction has the           following charactershics :-i if follow…

Q: 6. Please draw out the mechanism for Pinacol rearrangement. (Note: carbocation rearrangement by…

A: The pinacol rearrangement is an acid-catalyzed process that dehydrates glycols and changes them into…

Q: H;0"/H;O/A HO.

A:

Q: H H H-O- ċ-H + :Br: н — Br : : OH : - -

A: In SN2 reaction, the nucleophile attacks on the substrate from the back side of leaving group and…

Q: 10. Draw a reasonable mechanism for the following reaction (cat. = catalytic %3D amount).

A:

Q: Draw the mechanism ffrom benzaldehyde to this using:   i)NaBH4 ii)TsCl, py iii)NaCN iiii)H+,…

A: Given,  The mechanism for target product formed from benzaldehyde by using  i)NaBH4 ii)TsCl, py…

Q: Draw the product of attached asymmetric epoxidation reaction.

A: A three membered ring that contains two atoms of carbon and one atom of oxygen is called as epoxide.…

Q: provide a reasonable mechanism for the following reaction CX НО, OH H₂SO4 (cat)

A: Basically this reaction ia used in protection of aldehyde and ketone in order to prevent the…

Q: Drag the appropriate items to their respective bins. CH3 CH= CH2 CH3 CH3CH(CH3)CH,NH2 CH3CH2COO…

A: Attacking reagents can be classified into two types  Electrophiles (E+)  Nucleophiles (Nu-)…

Q: 3/5 5.1 each indicated reaction. Mechanisms. Using curved arrows, suggest a reasonable mechanism for…

A: The reaction of alkene with phosphoric acid leads to the formation of carbocation. The oxygen of -…

Q: H OH + H-CI = `CH, CH,

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Q: prese Maxwell Draw the major organic product of the reaction shown. Select Draw Rings More HI H3C-OH

A: in nucleophilic substitution reaction nucleophile attacks on substrate and forms product.

Q: (a) Arrango the tollowing intermediate in order of decreasing stability. Justity your answer. CH…

A: Here we have to write the decreasing order stability of the following given carbon free radical…

Q: Provide a curved arrow mechanism for the following reaction. CH;CH>OH + enantiomer

A: This reaction follows SN1 mechanism, In SN1 mechanism firstly leaves group leaves and carbocation…

Q: 10. (8pts each) Rank the reactivity toward the SN1 mechanism. Place answers in the box provided. CH₂…

A: Concept:  SN1 reaction: SN1 reactions are nucleophilic substitutions, involving a nucleophile…

Q: Which is the product of the reactuon sequence? P(Ph n-BuLI CH,CH,CH,Br OCH CH2CH он CH,CH2CH…

A: Given reactant molecule is:

Q: Arrow-pushing Instructions MeOH Draw curved arrows to show the movement of electrons in this step of…

A: Given reaction is :  Draw the curved arrows to show the movement of electrons in this step of the…

Q: 4. For the following, a) predict the product and b) using curved arrows to show electron movement,…

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Q: CH3 H;C-C-i: CH, CH3 H,C CH,

A: SN1  stands for nucleophillic substitution reaction where rate of the reaction depends on only the…

Q: Draw an arrow-pushing mechanism for the reaction below. Draw in all lone pairs and t may be present,…

A: Conversion of alcohol to alkyl halide with HCl reaction is carried out by carbocation…

Q: In the given condensed formula, I understand that there will be a carbocation rearrangement due to…

A: The E1 mechanism of conversion of secondary alcohol to alkene is given in step two.

Q: 5. Rank the following according to increasing reactivity (1- least reactive, 4 – most reactive in a…

A: The question is based on the concept of organic reactions. We have to identify the reactivity order…

Q: Add curved arrows to draw the first part of the mechanism: tautomerization of a ketone to an enol.…

A: A mechanism of an organic reaction is shown by the movement of electrons. An arrow is used to show…

Q: Show the complete mechanism for the formation of a hemiactetal, when 3-methyl-2-butanone eacts with…

A: Ketone with 1 equivalent of alcohol in acidic medium forms hemiacetal.

Q: Add curved arrow(s) to draw the final step of the mechanism. 18rt Br 3-3 CH₂ H₂C Br H₂C

A:

Q: 3) Write a detailed mechanism of: CH CH. HNOT H'SO NO

A:

Q: MENH2 SO3ME MеHN. NEC- CI NEC a. Draw a reasonable arrow-pushing mechanism for this transformation.…

A: There will be removal of HCl.

Q: (d) Explain the observed stereo-selectivity in the formation of product using Chelation model. OMe…

A: The mechanism of this reaction is done in the below.

Q: Add any remaining curved arrow(s) to complete step 4 of the mechanism. Modify the given drawing of…

A: The reaction mechanism step given is,

Q: H3C 0-CH3 H3C-o o-CH3 H3C- OH но CH3

A:

Q: CH3 + a13- 29°C

A: The key step in this transformation is the formation of a stabilized anion by using pyridine and…

Q: (5 points) What hydrolysis products are formed when the following compound is treated with aqueous…

A: This Compound is Acetal because it's have diether both and this Acetal Compound Hydrolyzed in the…

Q: Draw a stepwise mechanism for the attached reaction, which results inring expansion of a…

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Q: Q2. For the reactions below, draw out the reactions as shown and answer the following questions for…

A: This reaction example of elimination reaction.