ОН 1) Hg(OAc)» Н-о 2) NaBH4 `H сyclohexene суclohexanol

Q: Q.7: From ethane prepare ethylene glycol.

A: To solve this problem we have completed the given conversion reaction of organic compound.

Q: Identify the type of reaction for the formation of (S)-2-butanol from (S)-2-bromobutane

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Q: What two alkenes give rise to attached alcohol as the major product of acid-catalyzed hydration?

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Q: For example, does the oxidation ofcyclohexyl methyl ketone form methyl cyclohexanecarboxylate or…

A: Ketones are hard to oxidize as they do not ha a H atom dire tally attached to the carbonyl group.…

Q: 18. The addition of H2O to ethene yields a molecule called: (a) ethanol (b) ethane (c) ethyne (d)…

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Q: Write chemical equation including reagent(s) and condition(s) for preparation of 2- pentyne from…

A: Hydration of alkynes takes place when alkyne reacts with water in presence of Sulphuric acid and…

Q: What orbitals (including the unhybridized) are used to form the carbonyl bond in 2- ethylpentanoic…

A: Hybridization is a phenomenon in which the mixing of same or nearly same energy orbital takes place…

Q: the following reactions of one mole of reactant, predict the product, including its structural…

A: ->H2 can reduce double bond and triple bond and form alkane.

Q: Draw structures corresponding to the following names: a) 1-chloro-2-propanone c)…

A: Given,

Q: Which of the following molecules would release the LEAST amount of energy when being fully…

A: The heat of dehydrogenation is basically means the enthalpy of catalytic dehydrogenation. In…

Q: what is the catalyst required for the sulfonation reaction of benzene?

A: •Sulfonation of benzene :  1. In organic chemistry,  sulfonation process is required for the…

Q: (B) a What alkane should be used to synthesize the 1- bromo -1- ethyl cyclohexane? Write a chemical…

A: Note: As per our guidelines, we are supposed to answer only one question in the multiple-choice…

Q: Why epoxides occur ?

A: Epoxides are cyclic moieties that contain 'O' as a hetero atom. Thus, they are categorized as…

Q: =) Discuss the effect of ring strain on the carbonyl stretching for cyclic ketones.

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Q: Comparing Two Different Methods of Hydration of an Alkene Draw the product formed when…

A: In hydroboration-oxidation reaction of alkene, a hydroxyl group is introduced to the carbon with…

Q: CI Cl, / CH,CI, НО

A: The organic compounds in which a C=C bond is present are known as alkenes. Alkenes undergo an…

Q: Cyclopropane decomposes fairly rapidly at moderate temperatures whereas cyclohexane is quite stable.…

A: Hydrocarbons are the compound formed by carbons and hydrogen through covalent bond. There are two…

Q: Draw a structural formula for the major organic product of the following reaction: CH2Cl2, + Br2

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Q: Phenol and other derivatives with a single hydroxyl group on the aromatic ring are not easily…

A: Oxidation is also defined as removal of hydrogen from a compound. Alcohol is converted into ketone…

Q: The initiation step in the autooxidation process of organic compounds involves the homolytic…

A: Autooxidation is the spontaneous oxidation of a compound by molecular oxygen, usually forming…

Q: Given the reaction: benzoyl chloride + acetic acid Draw the structure of the tetrahedral…

A: Step 1:Step 2:Step 3:Formation of Tetrahedral Intermediate:The lone pair on the oxygen of acetic…

Q: Provide the major organic products(s) of the react Br CH3ONA

A: In the above reaction, the alkyl halide reactant given is a secondary alky halide i.e the carbon…

Q: When 30 cm3 of a gaseous hydrocarbon was exploded with 210cm3 of oxygen the residual gases occupied…

A: Values given in the question are as follow: Volume of unburnts oxygen is 30 cm3   the residual gases…

Q: This reaction mechanism is the proposed explanation for the preparation of alkenes from the organic…

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Q: 3-methyl-3-pentanol and phosphoric acid (alcohol dehydration)

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

Q: Compounds with more than one hydroxyl group can react with thionyl chloride differently from simple…

A: One hydroxyl group  reacts with thionyl chloride and oxidises alcohol to corresponding aldehyde or…

Q: What are the coefficients in the balanced equation for the complete combustion of…

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Q: y isomers can be formed in each case? (2) Addition of HBr to 3,3-dimethyl-1-butene gives a mixture…

A: The addition of particular group without any substitution. For eg., HBr addition in a double bond.

Q: complete the table by suggesting chemical tests to differentiate the following compounds and write…

A: NOTE: please note according to our policy , we can only answer first three subparts of a question.…

Q: Draw a structural formula for the product of the acid-catalyzed hydration of 1-methylcyclohexene.

A: Given: The compound 1-methylcyclohexene undergoes acid-catalyzed hydration.

Q: Indicate the products obtained when reactinga) Ethyl ethanoate b) Ethyl benzoatewith 1 or 2 (in each…

A: When reacting esters with Grignard reagents, such as methylmagnesium iodide (CH₃MgI), the reaction…

Q: Ketones serves as intermediate during oxidation which ultimately forms carboxylic acids from primary…

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Q: Explain the General Features of Suzuki Reactions with Pd Catalysts ?

A: Suzuki reactions are the coupling reactions in which there is the coupling of an aryl or vinyl…

Q: Explain this ? "Organic synthesis is the systematic preparation of a compound from areadily…

A: Introduction: In an organic synthesis, generally a small compound is taken and step by step after…

Q: Write the reaction for the formation of 1,4-di-t-butyl-2,5-dimethoxybenzene.

A: Synthesis of 1, 4-Di-t-butyl-2, 5-dimethoxybenzene in terms of Friedel-Crafts Alkylation

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.