2. Show how to make the following compound from propene?

Q: 3. How could you make the following compound from benzene or toluene and anything else you need? (…

A: To synthesize  from benzene.

Q: хаана NH₂ 1) SOCI2 2) PhMgBr 3) H30+

A: The question is based on organic reactions.We need to identify the product and explain its…

Q: Starting from cyclohexanol, show how to prepare: OMe (racemic) "OMe Show all reagents and molecules…

A:

Q: How can you prepare caproic acid from 1-butene?

A: We will synthesise  caproic acid from 1-butene.

Q: The following molecule can be synthesized from an epoxide and alkyllithium reagent, followed by…

A: Alcohols can be prepared from an epoxide by reacting it with an alkyl lithium reagent, followed by…

Q: CO2H SO3H Br

A: Synthesize the tri-substituted aromatic compound shown below starting from toluene. In this, we must…

Q: ...ОН

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

Q: 2. How would you prepare propyne from the following starting materials. Show the appropriate series…

A: We have to synthesized propyne from proan-2-ol.

Q: How could you prepare cis-3-hexene oxide from ethyne? (Show all reagents and intermediates).

A: In this process conversion of ethyne cis-3-hexene oxide. Find out intermediate and reagent

Q: Hiii!! Can somebody here help me with what my tutor made me? I can't really understand it…

A:

Q: OH 1. Hg(OAc)2. H20 2. NABH,

A: Product can be synthesized from the reaction of an alkene with Hg(OAc)2 followed by reduction with…

Q: Provide a reasonable route to synthesize the following product from the given phenol. Show all…

A: The given reactant is a m-bromo phenol and the product is m-alkyl substituted phenol. So, we can…

Q: Provide the reagents for the short synthesis (3 steps).

A: Propyne is a terminal alkyne it has acidic hydrogen , when it is treated with strong base like…

Q: What reagents would you use, and in what order, to convert ethane to propyne?

A: Ethane is an alakne, Saturated compound Propyne is alkyne ,unsaturated compound   ethane to ethyne…

Q: Provide syntheses for this compound. Your starting materials should be benzene, toluene and ethanol.

A: In this question, we will synthesized the final organic product from the given starting materials (…

Q: Which of the following reagents do not react with ketone carbonyls (Question 3)

A: Please find below the reactions taking place with each reagent

Q: How do you synthesize a cyclohexane-1,2,3-triol from a cyclohexane

A:

Q: Starting with benzene, propose a synthesis for the following compound: Br

A: We can synthesize the given molecule from benzene in the following way. At first, benzene undergoes…

Q: A student wanted to try to make phenoxyacetic acid using hydroxyacetic acid (HOCH2COOH) and…

A: Phenoxyacetic acid can be prepared by using hydroxyacetic acid (HOCH2COOH) and NaH. Strong base NaH…

Q: SYNTHESISI Show how the compound below can be synthesized efficiently from benzene, propane, and any…

A: Applying concept of organic synthesis.

Q: How would you synthesize the following compounds from cyclohexanone using reagents from the table?…

A: Answer is explained. Explanation:

Q: b) Br

A: When alkyl bromides are treated with a base, sodium ethoxide produces alkenes as the product by…

Q: ways ma starting materials and reagents. a cuprate an alkene an alkyne an alkyne

A: The given reaction involves the synthesis routes for certain compound from the unknown starting…

Q: Predict products: CH3)2CHMgBr CH3Li + + CH3CH₂MgBr + CH3CH₂MgBr + HO exces

A: Reaction involves the Grignard reagent with functional groups such as epoxide, alcohol, aldehyde and…

Q: 1) NaNH, 2) CH3CH₂Br

A: We have given the organic reaction and we have to find out product of the reaction.

Q: PPH3 B

A: Ans

Q: 9. Starting from benzene and using any necessary reagents, synthesize the following compounds. CI…

A: These are simple questions of reagent and reaction mechanism of organic reaction.

Q: HO

A: We have to make this reduced compound from benzene. For that, at first, we have to make benzoic acid…

Q: 1. Complete the following transformation, show step-by-step scheme "iy" H H H AND

A: The above given formation of products from the provided starting materials can be carried out in…

Q: Show how the following compound can be synthesized from benzene.

A: Friedal Craft Alkylation: The addition of an alkyl group in the presence of Lewi acid is called…

Q: OH O,N NH2

A:

Q: Each student must choose and analyze three of the four reactions: Rxn 1: Prop-1-yne reacts with H2…

A: 1. Alkyne reacts with hydrogen in the presence of palladium on a carbon catalyst to form an alkane.…

Q: 5. Propose a sequence of reagents to synthesize the following from benzene. Include the structures…

A:

Q: How would you synthesize the following compounds from cyclohexanone using reagents from the table?…

A:

Q: 3. Propose a synthesis to make the following products from the starting materials shown.…

A:

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.