[1] CH;0- [2] CH;OH

Q: Please correct answer and don't use hend raiting

A: Michael Addition:The Michael acceptor is a conjugated enone, such as methyl vinyl ketone (MVK).The…

Q: cat. H+ excess CH3OH -H₂O

A: Lone pair of ketone abstract proton to make Carbonyl more electrophilic .

Q: Glucose and galactose Energy of activation with lactase Energy Lactose and water Energy of…

A: Answer: In this question we have to mark the energy profile of the hydrolysis reaction of Lactose,…

Q: a) draw the product of this step b) is the alkyl halide the electrophile or the nucleophile

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Q: Please drau the Fouooing in the most Stable chair Form.Ju8tih Strueture your chobre. HO

A: The substituents in the chair form of cyclohexane experience unfavourable 1,3-diaxial interactions…

Q: TH.

A: Given images are : Increasing order of rate of nucleophilic addition = ?

Q: A nitrile LIAIH,/ether CIH

A: LiAlH4 reduces nitrile to primary amine.  Since, H- from LiAlH4 attacks on the sp- carbon of nitrile…

Q: Draw the complete, detailed mechanism for the reaction shown here and draw the major organic…

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Q: Please draw arrow-pushing reaction mechanism and identify number of electrons involved here. This is…

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Q: Draw the products of attached reaction by following the curved arrows.

A: The products of attached reaction can be drawn as

Q: Bonus: What anion is a more reactive nucleophile? Why? Must draw a picture! VS.

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Q: Step 1 Step 2 Step 3 Step 4 i Draw H3CH2C¯, and then add the curved arrow notation showing a…

A: Nucleophilic reactions are those reactions in which a nucleophile attacks the carbon of carbonyl…

Q: Please correct answer and don't use hand rating

A: Answer: The structure of the product The reaction: The bonds which are broken and which are formed…

Q: Please draw the possible products of the compund using radical reaction conditions. This is a…

A: A question based on reactions of alkenes. The possible product of monobromination under radical…

Q: Please correct answer and don't use hend raiting

A: Step 1:We have to give reaction. draw the product of the given Given:Explanation:>The given…

Q: The attached reaction does not afford the major product that is given.Explain why this is so, and…

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Q: Try It Draw the complete, detailed mechanism for the reaction shown here and draw the product.…

A: The reaction is a nucleophilic addition of carbonyl compound. The nucleophile -SCH3 adds on…

Q: „NO2 ÓTM ZI

A: Michael addition is the 1,4 nucleophilic addition of active methylene group compounds  across alpha…

Q: Apply Mechanism CH Hint Solution 11 remaining step(s) can be solved 4 possible noxt atops unlocked…

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Q: Please help me with a possible drawn synthesis for the shown reaction. Carbons should come from…

A: Step 1: Step 2: Step 3: Step 4:

Q: :):):));;$:&:&$:

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Q: Devise a synthesis of attached compound from an alkyl halide using anyother organic or inorganic…

A: The Williamson ether synthesis is a method for the synthesis of ether which occurs by an SN2…

Q: draw a curved arrow mechanism for the following reaction. You may use generic acids and bases to…

A: Given reactionTo draw a curved arrow mechanism for the following reaction

Q: Show the first step in the hydroboration mechanism using the reagents below.

A: In hydroboration - oxidation of alkene , there occur addition of H2O (anti-markonikov's addition) In…

Q: alDraw the complete mechanisms for this reaction ojű of zor b With reference to your mechanism,…

A: This reaction is an example of acylation of enamine

Q: Consider the mechanistic step shown below. Which of the four characteristic patterns of arrow…

A: We have to predict:  Arrow pushing pattern  Place for Head of curve arrow.

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.