heat benzaldehit + KCN + E1OH –→

Q: Complete the following reaction by adding major product. „Br + NAOCH3 CH,OH (solvent) hv • Br2 c)…

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

Q: Please show a detailed mechanism for the cleavage, in base, of propylene oxide, CH3-CH-CH2, to…

A:

Q: Give the major product (16) and the mechanism for the elimination reaction given below.

A: In this question, we will draw the major product with mechanism and explanation.  You can see the…

Q: 2) Write a detailed mechanism for the following reaction: он H30* OH

A: we have given that acid catalyzed epoxide opening to give diols.  the details mechanism of reaction…

Q: 3. Please provide a complete step-wise synthesis of the target molecule showing all steps, reagents…

A: Benzene on F.C.Alkylation to form Methyl benzene (Toluene) in first step. Then Toluene undergoes…

Q: DMSO 0

A:

Q: Write a mechanism for the following reaction

A: The details solution for this is provided below in attach image.

Q: step-wise mechanism (showing the movement of all electrons) for the following reaction :a HBr HO2 +…

A: In presence of peroxide, the negative ion goes to the less substituted C of the alkene.

Q: Provide the mechanism for the 4th and final reaction in this synthesis: КОН/D20 D FHN- OH

A: Answer

Q: 3-) Show the mechanism by using curved arrows for the reaction between following lactone and…

A: Grignard reagent first attacks the C=O of the cyclic lactone through nucleophilic addition reaction…

Q: The reaction below precedes via an E2 elimination versus an SN2 reaction. Circle all of the answers…

A: Elimination reaction are organic reaction where the certain functional group is lost to form…

Q: III. Which alkyl halide in each of the following pairs will react faster in an SN2 reaction with OH?…

A: The nucleophilic substitution reaction involves the removal of the leaving group with its bonding…

Q: What is the predominant mechanism of the reaction below?

A: Elimination reaction :   Inpresence of strong base , heating conditions elimination reactions…

Q: Why doesn't iodoethane react via Sn2 with NaI in acetone? It is a good leaving group and it is on a…

A: 1 .Nature Of Solvent Solvent SN1 SN2 Polar Aprotic Solvent (Acetone)   SN2 will favor Polar…

Q: Suggest a mechanism for the following reaction. Explain why NaB(CN)H3 is preferable to NABH4 as…

A: We have to suggest mechanism for the following reaction in step 2

Q: the dehydrohalogenation (E2) reaction, d

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Q: Propose a plausible mechanism for the following transformation. 1. OsO4 2. H3O*

A: Osmium tetra oxide is used to form vicinial diol on alkenes. After that pinacol-pinacolone type…

Q: Provide a plausible arrow pushing mechanism for the reaction below. OH LOME TSOH, H20 OMe

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Q: Write a detailed mechanism for this transformation. OH HCI НО НО H2O -OH

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Q: HO NH2 H3O+ HO NH HO Но

A: 4-(2-aminoethyl)bnzene-1,2 diol reacts with acetaldehyde in the presence of acid, it results in the…

Q: SN1 reactions are better performed in protic solvents. Explain why the researchers could not perform…

A: In SN1 reaction, alky halide/sulphonate react with a weak nucleophile. In first step of reaction…

Q: Give all the reagents, in order, that lead to forming the product.

A: Given reaction, Butane to 1-butyne

Q: What organic product is formed in the following reaction? (Note: here an ethyl group is not a…

A:

Q: Show the reaction mechanism for the formation of: a. RCONH2 from the reaction of RCOOR’ with NH3

A: given find mechanism of RCONH2 from the reaction of RCOOR’ with NH3

Q: ОН НІ, Н,О CH;CHCH3 ICH2CH3 + heat

A:

Q: Reaction 1: Reaction 2: CI CI AICI3 AICI3

A: Friedel craft reaction- Benzene is a nucleophile and addition of electrophile does not takes place…

Q: 3. Explain what the evidence tells you about the type of mechanism either Snl or Sn2 A. The rate…

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Q: Write a detailed mechanism for the following reaction. KCN. HCN

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Q: froblem of The Day1 Suggest an eficient synthesis for the following Transformation and provide a…

A: The addition reaction of alkene takes place when it is treated with Br2. The mechanism of the…

Q: OEt 1. NaOEt 2. H3O*

A: The given reaction is,

Q: 2) Write a detailed mechanism for the following reaction: H2SO4 CH;CH,C=CH + H2O CH;CH,CCH3

A: Hydration reaction of Alkyne takes place in acidic medium as follows:

Q: 2. Answer ALL parts. a) Write a detailed reaction mechanism for the following conversion. он Acetone…

A: Here we have write the reaction mechanism of following given conversion.

Q: Propose a mechanism for the following reaction:

A: The chloroform reagent taken is attacked by the electron rich double bond from the octadiene.

Q: Provide a plausible arrow pushing mechanism for the reaction below. OH OMe TSOH, H20 OMe

A: The answer is mechanism

Q: Draw a detailed mechanism for the chlorination of benzene using Cl2 and FeCl3.

A: The general reaction is as follows,

Q: Account for the following:  In a polar solvent such as water, the SN1 and E1 reactions of a…

A: Nucleophilic substitution The substitution reaction in which a nucleophile is substituted to form…

Q: Provide a plausible arrow pushing mechanism for the reaction below. You may abbreviate the…

A: The reactions follow (2π+4π ) cyclo addition Diels elder reaction. The first step shows Diels -alder…

Q: From the two synthetic routes shown below which one would be the best route for the desired product.…

A: 1) the reaction of cyclohexane react with NaBH4 to give cyclohexanol. because the NaBH4 is reducing…

Q: 4. Provide a detailed, stepwise mechanism for the reaction below. (CH3)2CHCH2CH2CH21 + CN- →…

A: Primary alkyl halide reacts with cyanide ion to form alkyl cyanide. The reaction follows the SN2…

Q: Stork developed the tollowing enamine reaction as an alternative to the Robinson annulation. Below…

A:

Q: Predict the product of this E2 elimination reaction. 1 ||| Br H3C Ph f Ph Ph H3C Ph Ph H CH3 Ph ||…

A: In case of elimination reaction , anti position of H and leaving group gets favourable . In this E2…

Q: 2. Circle the member of each horizontal pair that undergoes the faster SN2 reaction with Na*N3 in…

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Q: Propose a mechanism for the following reaction:

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Q: CH3 CH3 Br FeBr3. HBr (а) Br2 ČH3 CH3

A:

Q: Under second-order conditions (strong base/nucleophile), SN2 and E2 reactions may occur…

A: Under second-order conditions (strong base/nucleophile), SN2 and E2 reactions may occur…

Q: A set of three nucleophilic displacement reactions is shown below: CH3 SOH CH3CH2ĊCH3 SN1 reaction

A: GIVEN

Q: Provide the mechanism for the 2nd reaction in this synthesis: D2S04 PSO4

A:

Q: 1. Excess LIAIH4 MeO НО 2. H2о

A: Given reaction: We have to write the mechanism of the reaction.