yine reasons why the Compound 3-bromo -3 ethyl heptane gives no reaction with putassium hyclroxide but bromo-propane does

Q: Having trouble and the answer I put is wrong.  Name the alkene below. Use ONLY E/Z designators to…

A:

Q: What product is obtained from the reaction of dichlorocarbene with cyclopentene?

A: A simple trick for this reaction is, just insert the dichlorocarbene into the double bond making it…

Q: The following compound is treated with excess K2Cr2O7. Provide the name of the product that would…

A: K2Cr2O7 is an oxidising agent. It oxidised secondary alcohol into ketone.

Q: For each compound, give the product(s) expected from (1) HgSO4>H2SO4@catalyzedhydration and (2)…

A: The compound considered is a cyclic alkyne that has a 10 membered ring structure.

Q: Why does cis-2-chloro-1-cyclohexanol not yield an oxide when reacted with a base

A: In the case of the cis-2-chloro-1-cyclohexanol, which when treated with the base, cyclohexane is…

Q: Give IUPAC names for the following structures: Include R/S designations as appropriate.

A: In this question, we have to find out the correct answer of given problem by the help of the…

Q: Which of the following compounds shown below is butylberizene? to

A: The IUPAC name of the compound given is butylbenzene.

Q: Prepare the following compounds starting with cyclopentene and any other reagents.

A: For the given problem we have to find out the reagent which we used to convert cyclopentene to four…

Q: Like alcohols, ethers undergo a cleavage by breaking a carbon–carbon bond between an alkyl group and…

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Q: Draw a structure for (E)-3-phenyl-2-propen-1-ol in the space below. Show stereochemistry only if…

A: The organic compounds in which two carbon atoms are bonded to each other by a double bond are called…

Q: The major product of the reaction of methylenecyclohexane with N-bromo-succinimide is…

A: The reason for major product of the reaction of methylenecyclohexane with N-bromo-succinimide is…

Q: Draw the structure of the following and exposed each compound to oxidation of…

A: Thiols are similar to alcohols. In thiol -SH functional group present and in alcohol -OH functional…

Q: An unknown alcohol C6H14O gave a rapid Lucas Test. It could not be oxidized easily, but upon…

A: DBE of the alcohol = (C+1)-H/2 = (6+1)-14/2 = 0.  Hence, it is an aliphatic alcohol.  According to…

Q: Draw the major product(s) of chlorocyclohexane and lithium diisopropylamide in tetrahydrofuran

A: LDA( lithium diisopropyl amide): The bulky isopropyl groups of LDA make the base more selective for…

Q: Provide the systematic name of the major product after 1-butylcyclopent-1-ene reacts with HBr.

A: Given information: Reaction of 1-butyl-cyclopent-1-ene with HBr

Q: If 1-bromopentane is heated in acetone containing NaOH, what is the alkane produced? Draw and…

A: Here 1- bromopentane is heated in acetone containing NaOH. Here acetone is a polar aprotic solvent ,…

Q: Write a stepwise mechanism for each of the following reactions. Explainwhy a more stable alkyne…

A: Given reaction,

Q: Give the balanced equations of the reaction of hexene/cyclohexene with the following in: • dilute…

A: Hexene and cyclohexene contain double bonds that can undergo many reactions.

Q: What type of reaction mechanism accounts for the reaction of an conjuagted diene with aqueous acid…

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Q: compound X TSOH compound Y Note: TSOH= Me- (Hint: consider carbocations) for ] OH

A: We have to write the mechanism of the conversation of compound X to compound Y. This conversion of…

Q: addition of HBr to 1-phenylpropene yields (1-bromopropyl) benzene as  only product, why

A: Addition of HBr to 1-phenylpropene yields benzene as only product because benzyl carbocation is more…

Q: Which reaction intermediate is formed when 4-methylcyclohexene reacts with Br2 dissolved in CCl4

A:

Q: Draw the structure(s) of the organic product(s) predicted when this compound reacts with NABH4,…

A: NaBH4 acts as a reducing agent in organic reactions. In presence of carbonyl groups, the BH4-…

Q: Draw the structure(s) of the major organic product(s) of the following reaction: Mg, dry ether -Br…

A:

Q: what condition would you need to promote an elimination reaction of an alcohol to obtain an Alkene?

A: To make alkene from any alcohol we need to perform dehydration reaction. Hence we will heat the…

Q: (a) When cyclopropane is treated with HI, 1-iodopropaneis formed. A similar type of reaction does…

A: We know that most of the cycloalkanes get precipitated in similar reactions when compared with…

Q: rovide an IUPAC name for each of the compounds shown. Specify (E)/(Z) stereochemistry, if relevant,…

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Q: Epoxidation is typically achieved by treating an alkene with: a. bromine b. NBS с. ТСРВА O d. BH3,…

A: Alkene reacts with each reagent differently to give different products. We will draw each product…

Q: Br Br (4R,5Z,8E)-4-methyldeca-5,8-dien-5-ol

A:

Q: What happens when the following is added to conc. Sulfuric acid? (a) Cyclohexane (b) Cyclohexene…

A: We have to tell the observation when we add cyclohexane, cyclohexene and toluene to concentrated…

Q: Addition of HCI to 1-methoxycyclohexene yields 1-chloro-1-methoxycyclo- hexane as the sole product.…

A:

Q: Which of the following statement(s) is/are correct about (inorganic benzen (1) It contains pn-dn…

A: Inorganic benzene is Borazine with molecular formula – B3N3H6

Q: ou wish to produce n-butyl methyl ether from n-butyl bromide and sodium methoxide.  Write a breif…

A: The reaction of butyl bromide with sodium methoxide is as proceeded:

Q: Reaction of 2-methyl-2-pentene with  reagent is regioselective. Draw a structural formula for the…

A:

Q: Indicate the letter of the correct answer and kindly briefly justify the letter of answer.…

A: We have to draw the product when cyclohexene undergoes hydrobromination as follows in step 2:

Q: Explain why a single pure product is obtained from hydroboration–oxidation of 2-butyne, whereas two…

A: Please find below the reaction mechanism. Since the 2 pentyne is an unsymmetrical alkyne, the…

Q: In principle, how many alkenes (including all stereoisomers) can be formed from the following…

A: Sodium methoxide is a strong base and it favors bimolecular elimination reaction (E2). In E2…

Q: at would be the major product when 2-iodopentane is involved in a dehydrohalogenation reaction?…

A: Dehydrohalogenation is type of elimination reaction that eliminates an hydrogen halide from the…

Q: Sinthesis of 2,3-diphenylquinoxaline: which produce as a by product? HCl NH3 H2 H2O

A: The structure of 2,3-diphenylquinoxaline is as follows:

Q: 1.What are the various ways by which alkenes may be synthesized?

A: Since we are entitled to answer up to 1 question, we’ll answer the first question as you have not…

Q: Explain why hexan-2-ol is formed as the major product when 1-hexene undergoes acid catalyzed…

A: Acid-catalysed Hydration of Alkenes by the addition of water molecule and strong acid,forms alcohol.…

Q: Write out all the isomers of the compound with molecular formula C,H1,0 Select the normal/ primary…

A: The formula of compound is C4H10O  Since the formula of alkane with 4 carbon is  C4H10    Hence the…

Q: Draw the cycloalkene that would react with the reagent given to account for the product formed. CH3-…

A: The cycloalkene which react with given reagent to give above product is given in attached image.

Q: 2-Methylhex-3-yne can be prepared by the reaction of an alkynide with an alkyl halide. Does the…

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Q: or the following reaction, List all expected organic and covalen For each organic product, write out…

A: Alkyl halides undergo nucleophilic substitution reactions in presence of weak base , where as in…

Q: Show has to convert 2-bromo-2,4-dimethylpentane into 2,4-dimethyl-3-pentanol using laboratory…

A: For the given conversion first of all the alkyl halide is converted into alkene and then the alkene…

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.