Suggest a product of the following reaction. HI is a very strong acid Ch3ch2Och2ch3+ 2 HI gives

Q: Give the product of the following reaction.

A: Given,

Q: Heating toluene in the presence of KMnO4 followed by acification with HCl, converts toluene into…

A: The question is based on the concept of organic reactions.   We have to convert the reactant into…

Q: Show how Fischer esterification might be used to form the following esters. In each case,suggest a…

A: The Fishcer esterification is a process in which there is a acid catalyzed nucleophilic acyl…

Q: Indicate how you could synthesize trans-chalcone.

A:

Q: Provide the product of the following reaction, by writing the nume O Br HOCH₂CH₂OH H₂SO4 Mg.

A:

Q: 1. HNO3, H,SO, 2. Fe, HCI 3. NANO,, HCI 4. HBF, 5. KMN04, A CH(CHS2

A:

Q: Show how Fischer esterification might be used to form the following esters. In each case,suggest a…

A: Given Data:           Show how Fischer esterification might be used to form the following esters. In…

Q: Starting from toluene, propose syntheses for ortho-, meta-, and para-chlorobenzoic acid.

A: The first step of the synthesis of ortho and para chlorobenzoic acid form toluene is shown below.

Q: 3. Write in the product of 3-isobutyl-1-heptyne with the following reagents: 1. ВНз 2. Н,Ог, "ОН 1)…

A:

Q: Propose an arrow-pushing mechanism for the bromination of trans-stilbene. Is the product a mixture…

A: Bromine on reaction with alkene undergoes addition reaction. The double bond present between carbon…

Q: Show how Fischer esterification might be used to form the following esters. In each case,suggest a…

A:

Q: 2. Suggest a plausible arrow-pushing mechanism for the base-catalyzed reaction of the arenediazonium…

A: Here the chemical reaction is:

Q: Predict the product of the following reaction: PHCH2OH + PCC in CH2C12 ->

A: PCC (pyridinium chloro chromate ) it is an mild oxidising agent.  It can changes primary alcohols to…

Q: The ketone shown was prepared in a three-step sequence from ethyl trifluoroacetate. The first step…

A: Ethyl Trifluoroacetate on reaction with NH3  give amide. Amides on reaction with Grignard reagent…

Q: Give equations to show the reactions of sodium stearate with the following.(a) Ca2+

A: INTRODUCTION: Sodium stearate molecular formula C17H35COONa.It is a sodium salt of stearic acid.It…

Q: Provide the structure of the main product.

A: In this question we have to tell the main product of the reaction.

Q: What will be the complete hydrolysis products of the given structure below?       yield 1 mole of…

A: The given compound contains ester bonds and these ester bonds are hydrolyzed into carboxylic acids…

Q: 1. PPH3 Br X reacts further with carbonyl- containing compound (not part of this question) 2. MeLi…

A: Alkyl halide reacts with PPh3 to give a phosphorous derivative. This on reaction with strong base,…

Q: CO2H CH3CO2H +

A: We have to propose the structures for hydrocarbons (and give the organic reaction) that give the…

Q: 4. Predict the biotransformation and conjugation metabolite of below molecule

A: Biotransformation is the alteration of molecule without breaking the bonds.

Q: Ilustrating with an equation show how oxirane can be converted to 1,2 -diphenoxyethane

A: The conversion from oxirane to 1,2, -diphenoxyethane is shown as,

Q: Synthesis of Hexyl Acetate via an Sn2 Reaction. DMF Br Heat

A:

Q: suggest an alkene that could be used to make each of the following halohydrins.

A: The explanation is given below-

Q: Suggest an acyl chloride that was used to make the following compounds: PHCOCH2CH2CH3

A: In the organic conversion, suitable reagent converts the reactant into products. Reagents attacks…

Q: Provide the structure of unknown compounds for the following reactions

A: 1. Final product is a 3o alcohol Ketone reacts with grignard reagent followed by  hydrolysis to give…

Q: Show the mechanism for the acid-catalyzed formation of 23c starting with the product obtained from…

A: Fischer esterification- When carboxylic acid is heated with alcohol in presence of concentrated…

Q: Fill in the missing reagents and intermediates in the synthesis of Lidocaine. Provide a detailed…

A: The solution is as follows:

Q: NaBH4 AICI3

A: The above reaction is an example of Friedel Craft acylation.

Q: B. Using curved arrows, show the mechanism for the formation of A-1 haloalkane through electrophilic…

A: Formation of haloalkane:

Q: HCN H3C CH2CH; KCN

A: Carbonyl compounds such as Aldehydes and Ketones when react with HCN/KCN form cyanohydrin products…

Q: Vancomycin is an important antibiotic. It is isolated from the bacterium Streptomyces orientalis and…

A:

Q: Provide the product of the following reduction of the reactant below

A: Since you have posted multiple questions, the answer for first question is given below. Kindly…

Q: 4.- Provide an example of the use of (S)-proline as organocatalyst, and mention how this catalyst…

A:

Q: Propose the structures for hydrocarbons (and give the organic reaction) that give the following…

A:

Q: Give the product of the following reactions

A: Nucleophilic substitution reactions are a type of organic reactions in which an electron-rich…

Q: Methyl salicylate cannot be produced by using methyl chloride through an SN2 process. Explain. What…

A: This can be explained by SN2 reaction mechanism

Q: NaOCH2CH3 LOCH2CH3 H3CH2CO

A: This reaction occur via intramolecular cleasion condensation reaction pathway.

Q: Predict the products  of the reaction of phenylaceetaldehyde , C6H5CH2CHO, with a. NaBH4 the H3O+…

A:

Q: why is the synthesis of NH4BF4 conducted under acidic conditions?

A: The synthesis of NH4BF4 conducted under acidic conditions as follows,

Q: (a) TBSO TBSO

A: H2/Ni or Pd or Pt

Q: Proline betaine is a putative osmoprotectant in plants and bacteria, helping to prevent dehydration…

A: Given compound:

Q: An unknown alkyl chloride, designated as compound F, forms a Grignard reagent which on treatment…

A: Organic reaction.

Q: Which of the follow produce benzoic acid on reaction with aqueous acidic Na Cr207 at reflux H3C…

A: Alkyl benzene reacts with chromic acid to form benzoic acid. Only primary and secondary alkyl…

Q: For the following reaction, provide an arrow-pushing mechanism and the product. Ph₂P. KOtBu e Br

A:

Q: Provide the product for the following reaction. to pyridine

A:

Q: H2Cro, A 2CH2CI2 B (i) 2Benzene AICI3

A: The first step of the reaction involves the friedal craft's alkylation reaction. In this reaction…

Q: Give the product of the following reaction

A: The given reagents sodium borohydride and Lithium aluminum hydride are both reducing agents that…