Draw the enolate anion and the carbonyl that would be needed to make this product through an aldol condensation reaction. si Draw Enolate Anion Q

Q: lly 애 I I D

A: Primary bromide first form a 1o carbocation in presence of silver which precipitate as AgBr. Then a…

Q: Explain why acetals do not react with nucleophiles.

A: Nucleophiles are electron-rich species. They have tendency to donate electron density. If any other…

Q: Draw the enolate anion and the carbonyl that would be needed to make this product through an aldol…

A: Aldol condensation is the condensation between two aldehdyes or two ketones having at least one…

Q: b. Show what combination of aldehyde, ketone, and/or ester can prepare each compound below. Every…

A:

Q: HO H2SO4 애

A: We know the epoxide are very strained, so it tires to open up is ring in presence of acid to release…

Q: Draw the major product of the following reaction sequence. OH H2CrO4 HO NaBH4 H*/H20 ELOH он H3C* но

A: Explanation step wise .

Q: Under acidic condition, the first step in the addition of a nucleophile to a carbonyl compound…

A: The nucleophilic addition to a  carbonyl compound involves the addition of the weak nucleophile to…

Q: 4. Draw the aldehydes needed to prepare the compound below by an aldol reaction. OH CHO From: ogyhnu…

A: In aldol condensation the carbonyl compounds containing alpha hydrogen are necessary for formation…

Q: HO HS

A: This is a simple reaction sequence where first step is fast acid-base reaction and the second step…

Q: Draw the hemiacetal intermediate and acetal product of the reaction.

A: Final answer is given in explanation please see from there.Explanation:Approach to solving the…

Q: Draw the enolate anion and the carbonyl that would be needed to make this product through an aldol…

A: An enolate ion is an anion formed by the removal of an alpha-hydrogen atom from a carbonyl compound,…

Q: Draw the self aldol product of the following reaction NaOH/H20 H. no heat

A: a.

Q: Draw both products for the following reaction. NaOH

A: When an ester reacts with NaOH it undergoes saponification forming a ssacarboxylic acid and an…

Q: Draw the complete mechanism for the acetal formation.

A: see the image belowExplanation:

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.