Apply Mechanism Hint Solution 2 remaining step(s) can be solved

Q: What is a multi-step synthesis with intermediate steps to produce the following molecule?

A: Multi-step synthesis of this molecule:The IUPAC name is 4, 5 dichloro 6, 6 dimethyl octane. The…

Q: Show the reagents and intermediate products in the forward direction

A: Conversion of alkyne to epoxide is given.We have to find the reagents and intermediate products in…

Q: Draw the following steps

A: We have to draw following given reactions in a stepwise as follows in step 2:

Q: HO 2. Complete the following reactions by filling in any missing reactants, reagents or products. a)…

A:

Q: 1. Nucleophilic addition involving H₂CO 2. Nucleophile elimination ?

A:

Q: S. H* v the protecting group reactant. ect Draw Rings More

A: When we used the retrosynthsis means reverse to synthesis then we can easily identify the reactant…

Q: Br- Draw the intermediate that reacts with halogen in this reaction.

A: Under basic condition the ketone gets deprotonated and forms enolate and then on attack of halogen…

Q: ts] Draw the mechanism for the reaction listed below. acetone benzaldehyde NaOH

A: Step 1: Step 2: Step 3: Step 4:

Q: H H N H H CL H H

A: Step 1: The strong nucleophile attacks on the electrophile which is alkyl halide. Step 2: leaving…

Q: Draw the product of attached reaction.

A: The mechanism is as shown below:

Q: Explain how to decide which mechanism(s) the reaction will follow including information about: o…

A: It preferred E2 reaction due to strong and bulky base

Q: 18. Draw the product of the following reaction. .CI 1. AICI3 2. H2O

A:

Q: Complete the synthesis. Show all major intermediates. ~

A: PCC oxidises primary alcohol to aldehyde and secondary alcohol to ketone.Hydroboration-oxidation…

Q: Complete the following reactions by providing the proper substitution AND the proper elimination…

A:

Q: Compare the following reactions. Which is faster? Using a Free Energy Diagram, justify your choice.…

A:

Q: Draw a stepwise mechanism using arrows to show electron movement and drawing each intermediate…

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: Draw reaction of an a,b-unsaturated aldehyde or a ketone with a nucleophile forms a direct addition…

A: Given reaction,     a,b-unsaturated aldehyde or a ketone with a nucleophile

Q: draw the step one product and draw curved arrows to show the nucleophilic addition step.

A: To provide the arrow mechanism for the first step of the Fischer esterification reaction and the…

Q: 0 0 8 2 :0–CH, Add/Remove step X

A: Product of following reaction can be made by applying appropriate reaction mechanism.

Q: Which is an acetal fundional grp?

A: Functional group It is an atom or group of atoms that are responsible for the characteristic…

Q: CI AICI3

A: Hh

Q: `H + НО add slowly

A: The given reaction is a base catalyzed crossed aldol condensation reaction, in which two different…

Q: A B

A: This is an elimination reaction.  Here HCl is removed or eliminated to get an alkene.

Q: Elimination reactions require a nucleophile base

A: Elimination reactions  require a nucleophile or base ? The answer and explaintaion of the question…

Q: Please explain why this reaction will NOT WWORK. NO2 1. HNO3, H2SO4, 2. EtCI, AICI3

A:

Q: MCPBA to Ph alkene

A: mCPBA is the short form of m-chloroperbenzoic acid. It reacts in a concerted way, that is,…

Q: 8) Show how the following conversions might be accomplished, including all reagents and…

A: The chemical reaction in which an alkyl magnesium halide reacts with carbonyl compound followed by…

Q: CHO CHO MeO

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

Q: ? H

A: The question is based on the concept of organic synthesis. we need to synthesize the product based…

Q: Br CH3OH

A:

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.