1. Draw the structure of 4-ethoxy-2,2-dimethyldecane.

Q: Draw the product that could be formed when 1,3- butadiene reacts with ethene.

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Q: Consider the reaction below. What functional group is present in the reactant; and, what type of…

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Q: 3-ene (E)-4-bromo-5-methylhept-4-ene (4) (6)

A: Structure of (E) - 4 - bromo -5 - methyl hept-4-ene is given in the below image

Q: In the past ether was used as an anaesthetic but has been replaced by safer compounds because it is…

A: Ether molecules have no hydrogen atom on the oxygen atom (that is, no OH group). Therefore it has no…

Q: Heats of hydrogenation for alkenes. Hydrogenation of alkenes and alkynes are exothermic. Compare the…

A: Heat of hydrogenation depend number of pi bond Heat of hydrogenation inversely proportional…

Q: Aniline, phenol, and cyclohexanol are all three examples of aromatic hydrocarbons. T/F?

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Q: 2. A student named a compound as 3,3-dimethyl-4,4-diethylcyclohexa-1,5-diene. Even though one can…

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Q: a Write the structural formula for the product of each reaction. H₂SO4 + HNO3 • Draw organic…

A: benzene is an important electrophilic aromatic substitution reaction that is widely used in the…

Q: d) CHy Name reactant: Name product: e) CH=C-CH + 2 HBr - CH-CH CHy Name reactant: Name product:

A: Markonicov rule: It's state that for an addition reaction the negative charge of addaative will add…

Q: ispunoduloo ounds? a. CH,CH,CHCHCH, CH2CH3 b. CH,CH,CH,ČHCH,CH,

A: The IUPAC name of all the compounds has to be given.

Q: 11. Draw 5,5-dichloro-1-pentyne

A: Given  Name of Compound = 5,5 - dichloro 1- pentyne  Structure = ?

Q: Draw an appropriate structure (R)-a-Bromobutyryl Chloride

A: Butyryl chloride is an organic compound with the chemical formula CH3CH2CH2COCl (contains 4…

Q: give structure and correct name 3-methylbutane

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Q: a) Draw the skeletal structure of 3-methoxy-4-methylpentanoic acid. b) Give the IUPAC name for the…

A: Cis - trans isomer - it is geometric isomer  Same priority group on same side - Cis Same priority…

Q: Draw the structures of the ff: (E)-4-ethyl-3-heptene 1-isopropyl-4-propylcyclohexene…

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Q: Draw the skeletal structure of (E)-4-ethoxyhept-2-ene.

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Q: A hydrocarbon with one or more of the above bonds.

A: Alkyne correct option is 4.

Q: PBr3 (phosphorus tribromide) converts alcohols into alkyl bromides. Define ?

A: Alcohols are the organic compounds which contain the -OH functional group. The OH group of alcohol…

Q: give structure and correct name for 1,3-dimethylbutane

A: Given compound is 1,3-dimethylbutane.

Q: Please provide detailed solution and give the explanation of correct and incorrect options....

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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.