For the compound below, show the products obtained from ozonolysis, followed by treatment with dimethyl sulfide.

Q: The product obtained when the compound below is treated with H20 under acidic condition and heating…

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Q: Starting from acetylene and alkyl halides not longer than 4 carbon atoms, show the synthesis of…

A:

Q: Predict the major products of treating the following compound with hot, concentrated potassium…

A:

Q: ! Which set of reagents (given below) would produce the products given in the following reaction?

A: We can see 2 double bonds in the reactant which got transformmed into epoxide

Q: Predict the major products of treating the following compounds with hot, concentratedpotassium…

A: The recation mechanism is as shown below:

Q: Show

A: 1- NaH, THF  2- CH3-CH2-Br

Q: From what aldehyde or ketone could each of the following be prepared by reduction with NaBH4 or…

A:

Q: Give the major organic product(s) that would be expected on reaction of 3-pentanone (shown right)…

A:

Q: The reaction of an aldehyde with an amine gives an imine, which upon reaction with the ketone below…

A: Mannich reaction: Amino alkylation reaction of an alpha acidic proton of a ketone with formaldehyde…

Q: Predict the major products of treating the following compound with hot, concentrated potassium…

A: The structure of isopropylbenzene is,

Q: a) но н sock pyridine h)

A: Since you have asked multiple questions, we will solve the first question for you. If you want any…

Q: What condensation products would you expect to obtain by treatment of Ethyl butanoate with sodium…

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Q: Predict the major products of treating the following compounds with hot, concentratedpotassium…

A:

Q: Give the product of the following transformation:

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Q: Give the expected products of lithium aluminum hydride reduction of the followingcompounds (followed…

A: (a)

Q: Aromatic substitution can be done on naphthalene. Treatment of naphthalene with concentrated H2SO4…

A: The two compounds are 1-naphthalenesulfonic acid and 2-naphthalenesulfonic acid. The sulfonation of…

Q: CO2H CH3CO2H +

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

Q: For the compound below, propose an efficient synthesis using diethyl malonate as a starting…

A: In this question, we will synthesized the given product by using diethyl malonate as a starting…

Q: Answer one question using any of the compounds below. Propose a synthesis, using pyridine as one of…

A: Here we have considered the synthesis of 81. 4-cyanopyridine from pyridine.

Q: Describe a sequence of reactions by which 3-heptyne can be straightforwardly prepared from…

A:

Q: Propose the reaction mechanism for the two possible products formation from the following reaction…

A: The two possible products formation from the reaction of acetophenone and butanal and their…

Q: Propose a synthesis route to prepare the following product from acetophenone. Note that more than…

A: We have to start with acetophenone to get the desired product.  Acetophenone has a benzene ring that…

Q: PROPOSE A MECHANISM FOR THE REACTION OF PYRIDINE WITH H2SO4 AND HNO3. ACCOUNT FOR THE…

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Q: Show the structure of the main product when 2,2-dimethyloxirane reacts in methanol - in the…

A: Epoxide on treatment with the base like CH3OH result in the ring opening. The products formed in the…

Q: Predict the major products of treating the following compounds with hot, concentratedpotassium…

A: Given: p-xylene

Q: Predict the products obtained from the reaction of triolein with the following reagents. ozone, then…

A:

Q: Show the two organic products generated when the trialkylborane is oxidized with H2O2/NaOH

A: The given reaction is a hydroboration reaction. The two organic products that are generated when the…

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

A:

Q: Give the products (if any) expected from the treatment of each of the compounds with ozone followed…

A: The solution is as follows :

Q: Show how you would synthesize the following:  2-phenylethanol from a suitable alkene

A: (b) The synthesis of 2-phenylethanol from a suitable alkene is given below.

Q: Which reactant will give the products shown below when subjected to acid hydrolysis?

A: Hydrolysis of cyclic ketal results in the formation of corresponding ketone and a specific diol.

Q: Give the major product of the following reaction

A: Given reaction,

Q: Provide a detailed, stepwise mechanism for the acid-catalyzed reaction of 2-butanone with ethylene…

A: The mechanism with all the proper steps has been explained in the image below.

Q: Use a sheet of paper to answer the following question. Take a picture of your answers and attach to…

A: The nucleophile is CH3CH2O-.  The reactant, a conjugated enone undergoes an addition reaction by the…

Q: Explain synthesis pathways of methyl salicylate from the simplest hydrocarbon. Gives 3 of them.

A: Benzene convert into methyl salicylate by different way.

Q: Show how you would synthesize the following:  3-cyclohexylpropan-1-ol by the addition of ethylene…

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Q: Consider the sequence of reactions below. In this sequence of reactions, an unsaturated ketone is…

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Q: Give

A: Reaction sequence is given in Image.

Q: Show how you would synthesize the following compounds, starting with benzene or toluene and any…

A: “Since you have posted a question with multiple sub-parts, we will solve first three subparts for…

Q: 2-Ethyl-1-hexanol was needed for the synthesis of the sunscreen octyl p-methylcinnamate. Show how…

A: (a) Addition reaction of ketones and aldehydes is an aldol reaction and it is reversible reaction.…

Q: The following product was obtained from the ozonolysis of an alkene followed by treatment with…

A: 1-methylcyclohex-1-ene undergoes ozonolysis followed by dimethyl sulfide to gives the structure of…

Q: Show how the following compound could be prepared by a Suzuki reaction (Bn = benzyl). OBn OMe BnO…

A: The given compound is To find: Preparation of the given compound using Suzuki reaction

Q: Show how the 2-phenylethanol can be prepared from benzene:

A:

Q: Propose a mechanism for the acid-catalyzed hydration of 3-methyl-1-butene to give 2-methyl-2-butanol

A: This conversion follows Markovnikov's rule. According to this rule, Hydrogen is added to the carbon…

Reactions of Ethers

Ethers (R-O-R’) are compounds formed by replacing hydrogen atoms of an alcohol (R-OH compound) or a phenol (C6H5OH) by an aryl/ acyl group (functional group after removing single hydrogen from an aromatic ring). In this section, reaction, preparation and behavior of ethers are discussed in the context of organic chemistry.

Epoxides

Epoxides are a special class of cyclic ethers which are an important functional group in organic chemistry and generate reactive centers due to their unusual high reactivity. Due to their high reactivity, epoxides are considered to be toxic and mutagenic.

Williamson Ether Synthesis

An organic reaction in which an organohalide and a deprotonated alcohol forms ether is known as Williamson ether synthesis. Alexander Williamson developed the Williamson ether synthesis in 1850. The formation of ether in this synthesis is an SN2 reaction.