which of these has tautorimzation occur during the mech of the final product

Q: Metal oxo reagents (like OsO4) are well-known to give syn dihydroxylation in their products (1).…

A:

Q: supply the missing product with all the mechanisims O Me2NH

A: Aldehydes and ketones react with secondary amines to form enamines. The reaction is catalyzed by…

Q: Draw the following mechanism. PLEASE DRAW

A: The nitrene undergoes rearrangement such that the carbonyl carbon of ester group migrates, followed…

Q: Provide synthesis pathway

A: The synthetic pathway of reaction with needed reagent provided below in attach image.

Q: Identify the cyclohexyl substrate which would undergo the fastest E2 with base.

A: E2 elimination is a one step concerted mechanism reaction in which dehydrohalogenation (or any other…

Q: Draw the major organic product (other than ethanol) formed in the reaction. Br CH3CH₂O- CH3CH₂OH…

A: We have to draw the major product of the given reaction.

Q: dibenzalacetone from acetone and benzaldehyde in ACIDIC conditions. PLEASE SHOW ME ACIDIC I GET THE…

A: Aldol Condensation  is an electrophilic substitution reaction at the alpha carbon in enolate anions.…

Q: Draw the complete, detailed mechanism (curved arrows) for the reaction between alanine and DCC and…

A: Step 1:Step 2: Step 3: Step 4:

Q: Name the mechanism and the draw the major product

A:

Q: How to draw the Mechanism When a Reaction Involves BothSubstitution and Elimination ?

A: Substitution reaction : The substitution reaction is the reaction in which the leaving group or a…

Q: CI (CH3)3CONa DMF ?

A: In the given reaction solvent is polar aprotic and base is strong and bulky. So, it will favor E2…

Q: 1. Acetaldehyde (2 carbon aldehyde) is being reacted with hydroxide in ethanol. The hydrogen alpha…

A:

Q: HO H2SO4

A: In elimination reaction a species leave the substrate and double or triple bond is formed.

Q: Br MeO, THE + NaOMe

A: Welcome to bartleby !

Q: Draw the major product of this elimination. Consider regiochemistry and stereochemistry. Ignore…

A: Given that, the reaction is:

Q: draw the mechanism with intermediates

A: In this question, we will draw mechanism with intermidiate. You can see details mechanism with…

Q: n micxed aldol condensation of acetone with excess benzaldehyde in the presence of NaOH. Draw the…

A: Aldol condensation takes place in those carbonyl compounds that have alpha hydrogen.  In the case of…

Q: When ethylbenzene reacts with bromine in a free radical halogenation, a small amount of product that…

A:

Q: Please Draw Mechnism and explain Biz FeBrz Все AIBN Brz A, hv why the are different.

A: For the first one :-

Q: н. CH3 CH3ONA H3C CH3 CH3OH

A: Epoxide openning in basic medium is the SN2 reaction .

Q: Identify the cyclohexyl substrate which would undergo the slowest E2 with base.

A: To identify the cyclohexyl substrate which would undergo the slowest E2 with base.

Q: Draw the major product of the aldol condensation reaction between two of these aldehydes with the…

A: This is an aldol condensation reaction.  Here simply two carbonyl compounds with having alpha proton…

Q: LHO AICI3 +

A: Phenol does not undergo  friedel crafts  acylation reaction. Acylation takes place at O atom of…

Q: In micxed aldol condensation of acetone with excess benzaldehyde in the presence of NaOH: it is…

A: We have to draw the result from a single condensation reaction when micxed aldol condensation of…

Q: Pls help ASAP on both.

A: Question 1 based on addition reaction of br2 Question 2 based find out type of arrow pushing

Q: Draw the major product of this elimination. Consider regiochemistry and stereochemistry_ Ignore…

A: The reagent CH3ONa is a base that is used to abstract H+ ions from the substrate. The given starting…

Q: Provide a complete arrow pushing mechanism for a single aldol condensation reaction between…

A:

Q: OMS CH2CH2OH ?

A: Substitution reactions are of two types i.e. SN1 and SN2.In SN1 formation of carbocation takes place…

Q: Draw all enols of the following ketone.

A: Keto form is more stable than enol form

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.