Write down the reagents (A and B) used and the mechanism for the following two steps!  Please answer the solution from the problem ( max in 30-45 minutes thank

Q: )CHz MgBY 2) AQ. Workup 3) PBY3 -CH3 Br

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Q: + i) +CH3-MgX H30

A: Grignard reagent :- Alkyl magn esium halide (RMgX)  is called grignard reagent. It is highly polar…

Q: With an example describe mechanistically how an extraction is carried out acid-base.

A: Acid-base extraction is employed to separate acidic and basic compounds from a mixture.

Q: Show the organic product formed when 4-methylpentanal is heated with sodium methoxide in methanol as…

A: We will find out the reaction product

Q: 2. Show the B-cleavage mechanism and product for following reaction -R R'

A: The given problem deals with β - cleavage reactions which are generally initiated in the presence of…

Q: show the major products and complete the mechanisms with proper arrow pushing notation.

A: The starting material in both the reactions is propene. The reactions are electrophilic addition and…

Q: Show the electron-flow mechanism of the chosen synthetic schemes. This involves predicting major and…

A: Benzene Sulfonic Acid to Phenol

Q: Identify which substitution mechanism best fits the following statement: The reaction proceeds…

A: A concerted reaction is a reaction in which all bond breaking and bond making occurs in single step…

Q: the 1-pentyne is reacting with CH3CH2CH2Li, then with the ketone, and lastly with NH4Cl and H2O.…

A: The solution of above question is-

Q: Draw curved arrows to show the movement of electrons in this step of the mechanism.

A:

Q: What is the correct mechanism and steps? Thanks

A: Hydrolysis of beta keto ester in acidic medium  producce ketone, CO2, alcohol in presence  of heat.

Q: NO2 NaOCH3 CI

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Q: Write out the reaction of Bromination of E-stilbene using chemdraw (ACS 1996 format). Include all…

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Q: -Name the correct mechanism via arrow pushing  -name each mechanism  -name each minor and major…

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Q: synthetic route + 0 |||

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Q: NaBr Acetone NACN DMSO NC NC EtzN: DMSO

A:

Q: What are the major product(s)? Show all the arrow push mechanism.

A: Biomolecular elimination (E2) reaction: E2 reaction involves a one-step mechanism in which…

Q: please probide synthesis for both problems H 2.

A: The alkene undergo oxidation reaction in presence of ozone followed by reduction with Zn/H2O to give…

Q: CH3,, CH2CH3 + H20 H20 Change the solvent (if it is protic by aprotic and vice versa). Draw the…

A: Activation energy is the minimum required energy to accelerate the molecules and atoms of reactants…

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

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Q: white reagents ب الله GH for each.

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Q: What is the major product(s)? Show the arrow push mechanism.

A: It is an example of E2 elimination reaction

Q: Provide a plausible arrow pushing mechanism for the reaction below. 1.1 eq. 1BUOK HO 2. acidic…

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Q: Please show the mechanism :) Thanks! H-

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Q: Show all the arrow mechanism including the PROPER reagents

A: Interpretation - We have to show the all the mechanism including the proper reagent in above…

Q: How is this incorrect and what is the correct mechanism?

A: Given : We have to tell what will be the correct mechanism.

Q: CH3 + НаС — сн н

A: We have to predict the mechanism for formation of given product via Michael addition.

Q: Give clear handwritten solution) give reaction mechanism and major product for the all three…

A: The Given question is various types Of bromination Reaction.

Q: Provide a plausible arrow pushing mechanism for the reaction below. 1.1 eq. tBuOK 2. acidic workup

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

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Q: Give mechanism of norrish type 1 reaction of cyclopentanone in gas phase and in solution phase…

A: Photochemical reaction occurs through radical intermediate.  In the both case alpha cleavage occurs.…

Q: down the product

A: Given:

Q: Show all the arrow mechanism including the PROPER reagents.

A:

Q: Show the electron-flow mechanism of the chosen synthetic schemes. This involves predicting major and…

A:

Q: Show retro-synthetic analysis leading from the target molecule to the precursor molecule showing all…

A: Given:- We have to transform the synthesis of given following below:

Q: Fill in the blanks: The E1 mechanism is most favored by a alkyl halide and a solvent.

A: E1 means elemination is Unimolecular and in this mechanism is most favourable in 3o type halocarbon…

Q: Please show mechanisms for following schemes

A: The mechanism of the following linear polymerization and the cross linked polymerization reactions…

Q: CH3OH, H*

A: Aldehyde react with alcohol to give hemiacetal when react with 1 equivalent.

Q: Provide a retrosynthesis (with complete reaction conditions) of the followingcompound from alkyl…

A: The retrosynthesis reaction takes place as follows :

Q: Can you explain the mechanism? Can you provide a shortcut?

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Q: Ph oH Ph propose a detariled mechanism, ysing (arNed arows to Show notation of flow of ckctrons.

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Q: Please give me the reagents and show the mechanism. Thank you so much.

A: These reaction involes the Michael addition reaction. Michael addition reaction involves the…

Q: Please show me the mechanism for O3+2-methyl-2-butene, stoping at the ozonide?

A: Ozonolysis is an organic reaction in which ozone is reacting with unsaturated compounds such as…

Q: Please help me with the a proposed Williamson ether  sysnthesisi for 3-ethoxyhexane. Thank you !

A: Williamson ether synthesis is SN2 reaction. This reaction is between alkoxide (deprotonated alcohol)…

Q: HiCan you help me solve this question?

A: Startinf from benzene as organic reagent and by using HNO2 and HBF4 inorganic reagent we can prepare…

Q: он CN

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: 1 Write a reaction mechanism for the following conversion, including reagents and/or conditions.…

A: Detail mechanistic pathway is given below to carry out the conversion

Q: I need help synthesizing metaxalone in a different way than it is patented to make. my starting…

A: To find out the starting materials, retrosynthesis analysis gas been carried out. The synthesis plan…

Q: Give the mechanism given bleow reactions with curved arrow and all format harges ? 1-ct y

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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.