Using only concentrated HCI, show the mechanism for the reaction shown below. OH HCI CI

Q: Propose a mechanism for the reaction. Fill in the missing curved arrows in each step.

A: The given reaction is of dehydration of alcohol to alkene

Q: (d). 1. MgBr 1. O3 (2 equivalents) 2. Me,s 2. H20

A: Organic compounds in which two carbon atoms of a hydrocarbon chain are bonded to each other by a…

Q: OH Propose a mechanism for the reaction shown here. Note that the reaction does not take place…

A: The mechanism for the given reaction is to be drawn. The reaction is, This is the epoxide ring…

Q: Product(s) (1) MeMgCl, Etz0 (solvent) Ph' Me (2) HCl(aq) "work-up"

A: We have to draw the product of the reaction below, including step by step reaction mechanism with…

Q: H. NH2

A: The reaction taking place is given as,

Q: Choose the correct mechanism for the following Syl reaction. + H,O + I- OH2

A:

Q: OH HO Br HO

A: The question is based on the concept of chemical conversions. we have been given reactant and…

Q: Show a possible mechanism for the following reaction 1) LAH (xs) 2) H3O* 3 MeOH

A:

Q: What are the major products of these reactions (pls show the mechanism so i can understand how to do…

A: Hello. Since the question contains multiple subparts the first three subparts are solved. In case…

Q: Show all of the steps in the mechanism for this reaction: CH3 CH3 CH;-C-CI CH;OH CH —С—ОСН, + HCI…

A:

Q: 3. Write the mechanism for the reactions below. Pd cat, base Br heat Et0OC Et0OC- Et0OC Et0OC

A: The mentioned conversation involves two major steps such as coupling process mediated by palladium…

Q: Provide the mechanism for the 2nd reaction in this synthesis: H2O CI

A: Step 1: Acid chloride reaction with Grignard will give the ketone. Step 2: keto compound react with…

Q: OMe cm Clz mCP BA MeO `OH

A: Given reaction is example of Baeyer-Villiger oxidation. The Baeyer–Villiger oxidation is an organic…

Q: OH OH ∞∞ BF3 Et₂O This reaction takes place via a pinacol rerrangement. Please, draw curved arrows…

A:

Q: Propose a mechanism for the reaction shown below

A: Please find below the reaction mechanism.

Q: of KOH / CH;OH HO,

A: Organic reaction mechanisms:

Q: H* 2. H2O

A: Alkene mainly gives electrophilic addition reaction in which an electrophile attacks on electron…

Q: Show a possible mechanism for the following reaction CN CO,Me CN.

A:

Q: Provide a complete mechanism for the following reaction. Use curved arrows to depict electron each…

A:

Q: H2SO4 OH

A: In the given transformation one acetal bond breaks and another acetal bond is formed:

Q: HO OH Br HO

A: synthesis of grignard reagent from alkyl halide attack of grignard reagent (as nucleophile) to…

Q: Show the product from the following reaction, and draw the reaction mechanism. CO₂H Br₂ NaHCO3, H₂O

A: The mechanism and the final product are given below,here NaHCO3 act as a base

Q: H2N. Br N° H2N

A:

Q: 3. Show the complete mechanism for the reaction below. H2N-NH2 NH2 • cat. HCI

A:

Q: Rank the following bases in order from slowest E2 reaction rate to fastest. ONa H20 NaOH NH3 OK ONa…

A: Nucleophiles which are strong bases are likely to undergo elimination over substitution. Bulky…

Q: Propose a mechanism for the Pictet-Spengler reaction, an example of which is shown here. Note that a…

A: Pictet- Spengler Reaction It is the condensation reaction between β-aryl ethyl amine with an…

Q: show me and explain the mechanism for this reaction please

A: In the above reaction, since the alcohol is 2 degree, hence the reaction is happening  The above…

Q: Heat Benzaldehyde + KCN + EtOH

A: Concept introduction: Benzoin condensation: It is the coupling reaction that is occur between the…

Q: CHO CHO MeO

A: Diels-Alder reaction: The Diels–Alder reaction is a pericyclic reaction (cycloaddition) between a…

Q: Finish the synthesis by listing out the reagents/solvents used and draw intermediate structures. You…

A: Here we have to synthesize 4-ethylcyclohexanone from given starting material.

Q: Can someone please show me a step by step mechanism of this reaction?

A: The given reaction is

Q: Draw the mechanism for the reaction below. OH HN. HCI H2O, heat OH NH₂ OH + Я OH

A:

Q: Meo ACOH MeO. NH2 NH

A: This is two step process. First step is the acid catalyzed imination of amine with aldehyde. second…

Q: NaH + H; + EO OH

A: NaH acts as strong  base and and form hydride ion, H- . It abstract hydrogen from alcoholic group.…

Q: НО H2SO4 heat

A:

Q: H3CO, NaOH H,CO H3CO OCH3

A:

Q: 15 EtgSiOTf (16) CH;CN OTf EtO EtO Show the mechanism for this reaction

A:

Q: .ce AICly

A: This is the friedelcraft reaction .

Q: Suggest a reasonable mechanism for the reaction shown Br here. HO CH;CH,OH

A: The given reaction is shown below:

Q: HO H, O

A: In this question, we will draw a mechanism for this reaction step by step.  Acetic anhydride is a…

Q: Show the step-wise mechanism for the thermodynamic product of the following reaction: HCI

A: Since you have posted multiple questions, we are entitled to answer the first only. The reaction…

Q: МСРВА H,OʻH,0 ? CH,Cl2

A: Please find the attachment

Q: CH3 CH3 from OH and isopropyl alcohol

A:

Q: Show all the steps for the mechanism for the problem below. This is an olefin alkylation and has 2…

A: The mechanism for the following reaction is shown as,

Q: Draw a mechanism for the reaction when the additive is added first, assume suitable aqueous workup…

A: This is an example of ortho lithiation reaction

Q: D. Provide a reasonable mechanism for the following reaction. ·CCL 3 1. NaOH, H₂O 2.H₂O* он

A:

Q: Show the mechanism of the following reaction. Br HBr Br

A:

Q: OH -NO

A: The question is based on the concepts of Organic reactions. we have been provided reactant.  we have…

Q: d) Write a mechanism for this reaction: AICI3 HCI + CH,Cl, CI

A: Organic reactions are those in which organic reactant react to form organic products.

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.