Give the structure of the major and minor organic products formed when HBr reacts with (E)-4,4-dimethyl-2-pentene or (E)-4,4-dimethylpent-2-ene in the presence of peroxides.

Q: Describe a sequence of reactions by which 3-methyl-1-butyne can be straightforwardly prepared from…

A:

Q: Name the possible alkenes which will yield 1-chloro-1-methylcyclohexane on their reaction with HCl.…

A: Well, we have to keep the skeleton as it is, which is basically the mehtylcylohexane.  And then we…

Q: Write the structures of all the alkenes that can be formed by dehydrohalogenation of the following…

A:

Q: Describe a sequence of reactions by which meso-2,3-dibromobutane can be prepared from propyne.

A:

Q: Compound X has molecular formula C7H14. Hydrogenation of compound X produces 2,4-dimethylpentane.…

A: Given molecular formula of compound X = C7H14So, compound X contains 1 double bond.

Q: Provide a series of synthetic steps by which (CH3)2C CH2 could be prepared from 2-methylpropane.

A: Interpretation-  To provide the synthesis steps by which (CH3)2C=CH2 could be prepared from…

Q: Give the structure(s) of the organic product(s) that would result from dehydrohalogenation of…

A: Dehydrohalogenation is an elimination reaction that eliminates i.e removes a hydrogen halide from a…

Q: Predict the b-elimination product(s) formed when each bromoalkane is treated with sodium ethoxide in…

A: beta-elimination: The elimination reaction takes place from beta-carbon of haloalkane is known as…

Q: An unknown hydrocarbon A with the formula C6H10 reacts with 1 molar equivalent of H2 over a…

A:

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

A:

Q: Draw the structure of each product from the reaction of benzene with 2-chloro-1-methylcyclohexane…

A:

Q: Predict the product formed in the nucleophilic aromatic substitution reaction between…

A: Nucleophilic Aromatic Substitution Reaction : is a Substitution reaction in which the nucleophile…

Q: Give the sequence of reactions that produce 2-bromo-4-ethylaniline from aniline. Draw the structures…

A: The molecule 2-bromo-4-ethylaniline contains an amine group which is ortho and para orienting. So,…

Q: Give the structures of the substitution products expected when 1-bromohexane reacts with(a) NaOCH2CH

A:

Q: What would the major organic reaction product be from the reaction of 1-bromo-1-methylcyclopentane…

A:

Q: Describe a sequence of reactions by which the aldehyde CH;CH;CH;CH;CHO could be prepared from…

A:

Q: What is the function of CH2Cl2 in the bromination reactions? Why

A: CH2Cl2  is the condensed formula of dichloromethane.It is commonly known as DCM.

Q: Mention and Write the following reaction mechanisms: a) thermal dehydration of 4-t-butylcyclohexanol…

A: Phosphoric acid is an acid that donates the H+ ion and oxygen of alcohol attack on this proton, H+.…

Q: Name (including E/Z stereochemistry) the five alkenes that can produce 3-bromo-3-methylhexane on…

A: Alkenes undergo electrophilic addition reaction with HBr to form alkyl halide.  The H+(aq) formed…

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: Predict the structural formula of the major product of the reaction of 2,2,3-trimethyloxirane with…

A: The reaction between  2,2,3-trimethyloxirane and ) Me2NH gives hydroxyl amines  Dimethylamine will…

Q: Provide the name of the product after heptanoyl chloride reacts with propan-1-ol under acidic…

A: The product of reaction between heptanoyl chloride and propanol can be predicted by its mechanism

Q: CH3 Br2/FeBr3 C3H,Bro 5 6 Using resonance structures, justify whether the acetyl group of compound 5…

A:

Q: What is the structural requirement for a substance to react with ammoniacal AgNO3? Why would…

A: We have been asked what is the structural requirement for a substance to react with ammoniacal…

Q: Acid-catalyzed dehydration of 3,3-dimethyl-2-butanol gives three alkenes: 2,3-dimethyl-2-butene,…

A: -> Reactant -> 3,3-dimethyl-2-butanol  -> Products-> 2,3-dimethyl-2-butene ,…

Q: Acetylacetone (pentane-2,4-dione) reacts with sodium hydroxide to give water and the sodium salt of…

A: The acetylacetone (pentane-2,4-dione) reacts with sodium hydroxide to give water and the sodium salt…

Q: Write a reaction that could be carried out to synthesize 1-(4-methylphenyl)ethanol (reactants will…

A: Grignard reagent is like RMgX where R = organic group and X = halide atoms.Carbonyl compound…

Q: The following alkyl halide can be prepared by addition of HBr to two different alkenes. Draw the…

A:

Q: Which alkene reacts with a red-brown solution of bromine to form 1,2-dibromo-1-ethylcyclohexane

A:

Q: Name, draw and describe the organic product of the reaction between 2-methylbut-1-ene and H2O in the…

A:

Q: Write the equations for the preparation of 1-bromobutane from :(i) 1-butanol (ii) but-l-ene

A: A chemical compound containing only carbon and hydrogen atoms attached through single bonds is…

Q: What would be the major product obtained from the reaction of Br2 with 1-butene if the reaction were…

A: This is bromination reaction. Alkene react with bromine to give dibromo compound

Q: The reaction of 1-bromopropane and sodium hydroxide in ethanol occurs by an SN2mechanism. What…

A: The reaction of 1-bromopropane and sodium hydroxide in ethanol occurs by an SN2 mechanism is given…

Q: Two products are possible when pent-2-ene is treated with HBr. Write the structures of the possible…

A: Given: To determine the possible products, when pent-2-ene is treated with HBr.

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.