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…
Suggest a product of the following reaction. HI is a very strong acid
Ch3ch2Och2ch3+ 2 HI gives
Step by step
Solved in 2 steps with 1 images
- The formation of Br2 from NBS first involves the reaction of NBS with HBr to form an iminol intermediate and molecular bromine. The intermediate then undergoes acid-catalyzed tautomerism to form succinimide, the byproduct of the reaction. Propose a curved-arrow mechanism for the conversion of NBS into succinimide that also accounts for the formation of Br2.Give two syntheses for (CH3)2CH¬O¬CH2CH3, and explain which synthesis is betterGive the product of the following reaction. HCI
- Treatment of pentanedioic (glutaric) anhydride with ammonia at elevated temperature leads to a compound of molecular formula C5H7NO2. What is the structure of this product? [Hint: You need to think about the reactivity not only of acid anhydrides but also of amides and carboxylic acids]Predict the products of the following reactions.(a) CH3CH2CH2CH2C‚N + CH3CH2MgBr, then H3O+Suggest a product of the following reaction. HI is a very strong acid. CH3CH9OCH,CH3 + 2 HI
- CH3 Ph3P-CHCH3 H3C H3C Aldehydes and ketones are converted into alkenes by means of a direct nucleophilic addition called the Wittig reaction. In the reaction, a triphenylphosphorine ylide, also called a phosphorane, adds to an aldehyde/ketone to give a four-membered cyclic intermediate called an oxaphosphetane. The oxaphosphetane is not isolated but instead spontaneously decomposes to release triphenylphosphine oxide and an alkene. Ph3P-CHCH3 H3C The ylide is formed by reaction of triphenylphosphine, a good nucleophile, with a primary alkyl halide in an S 2 reaction, followed by deprotonation of the carbon with a strong base, such as butyllithium. The carbonyl carbon and the carbon originally bonded to the halogen become the two carbons with the double bond in the product alkene :0: CH3 Com The real value of the Wittig reaction lies in its ability to yield an alkene of predictable structure, as the C-C bond is precisely where the C=O bond was in the reactant and no isomers (other than…Give the product for the following reactions(ii) The elimination reaction between 2-bromobutane and NaOCH2CH3 gives two organic products. Draw a mechanism for the reaction which produces the major organic elimination product and provide a rationale as to why that is the major product.