21) Carbocation forms in the reaction of: A) SN1 B) SN2 С) Both D) Cannot determined

Q: Draw the structure(s) of the major organic product(s) of the following reaction. aqueous H,SO, KCN

A:

Q: Which energy diagram belongs to the reaction of alkyl halide RCH2Br and potassium hydroxide in…

A: When primary alkyl halides react with KOH in presence of THF (non-aqueous medium), the alkyl halide…

Q: the reaction of potassium permanganate with a hydrocarbon, it usually is converted to MnO2. What…

A: KMnO4  potassium permanganate when converted to MnO2 we can find oxidation number of Mn in potassium…

Q: What is each compound’s systematic name?

A: The given compound is shown below,

Q: Question 5 Which onels) of these is/are aromatic? D OC OB O none of them O Band D O Aand C O A, B,…

A: Those compounds which have Following properties are Present, are called aromatic compounds - (1)…

Q: The substitution product for the reaction Nat *OCH3 is Br

A: We have given the organic reaction in which the alkyl halide react with sodium methoxide we have to…

Q: Under certain reaction conditions, 2,3-dibromobutane reacts with twoequivalents of base to give…

A:

Q: What is each compound’s systematic name?

A: The given compound is a tertiary amine with two methyl groups and one cyclohexyl group. The IUPAC…

Q: Which of the following alkene addition reactions is regioselective? A) Halogenation B) Hydration C)…

A: In this question, which process ( Halogenation Hydration ) Alkene addition Reaction is…

Q: Question 21 Place the carbocations in order or increasing stability. (least stable listed first) C…

A: A<B<C

Q: Explain why the addition of HBr to alkenes A and C is regioselective, forming addition products B…

A: Since in case of A, the product formed is because the stability of +ve charge will be more at the…

Q: Which of the following concepts explains why a tertiary carbocation is more stable than a primary…

A: We have to say why a tertiary carbocation is more stable than a primary carbocation?

Q: Select the meta-substituted dibromobenzene Br Br Br Br Br & & & & Br Br Br A B C D

A:

Q: The antispasmodic drug biperidin is made by the Grignard addition reaction shown here. What is the…

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Q: How is alkyne prepared by Kolbe’s method?

A: Alkyne is referred to any chain of unsaturated hydrocarbons having triple bonds such as acetylene.

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: explain electrophilic substitution reaction with example.

A: The replacement of any atom or group of atoms by an electrophile is termed as electrophilic…

Q: 1) LIAIH, HCI, H2O Y EN 2) H2O

A:

Q: Give systematic names for the following compounds: (а) (b)

A: Select the carbon chain containing functional group i.e. the principle chain  Numbering  Naming…

Q: Which statement is true about the isomerization reaction below? catalyst O The use of the catalyst…

A: Isomerisation reaction is the conversion of one isomer into another isomer. Trans form of alkene is…

Q: Br No reaction occurs when benzene is treated with Br, in CCI4. When anthracene is treated with Br,…

A:

Q: 1) OsO4 2) NaHSO;/H,O 1) O3 B + C 2) Zn/HOAC

A: A. Alkene on reaction with OsO4 followed by NaHSO3 gives cis-diol via the formation of five membered…

Q: Draw the structure(s) of the major organic product(s) of the following reaction. H,PO2 CH3

A: In the first reaction, the diazonium salt is reacting with H3PO2 and in the second reaction an amine…

Q: What is more stable acetate (CH3COO-) or ethoxide (CH3CH2O-)? In three words or less explain your…

A: Stability of anion: Primary carbanion is more stable than secondary and tertiary carbanions due to…

Q: H2 Lindlar's catalyst Both A and C A. С. D. B.

A:

Q: How to prepare dicyclopentylether from cyclopentene??

A: Preparation of dicyclopentylether from cyclopetene

Q: 20) Which of the following statement(s) is(are) TRUE? a. Hydrogenation and combustion of alkenes are…

A:

Q: КОН CH3(CH2)16C ОН

A: The given compound is an acid. It will react with KOH to given potassium salt of acid and H2O.

Q: ving free radicals is the MOST stable? C. D.

A:

Q: What is the major substitution product to the following reaction? Но OCH,CH3 Chapter 9 Homew..pdf…

A: Option 2nd will be correct.

Q: Consider the following alkyl halide compounds. CH3CH2CH(CI)CH2CH3 CH3C(CH3)(CI)CH2CH3 CH3CH2CI…

A:

Q: Write the IUPAC name of   compound, showing stereochemistry where relevant.

A: Carboxylic acid is a functional group in which the -COOH group is directly attached to the…

Q: QUESTION 3 Use Hammond's postulate to determine which alkene in each pair would be expected to form…

A: Hammond's postulate suggests that the stability of carbocation reactive intermediate has a direct…

Q: Determine the structures of compounds A and B in the following reaction scheme.

A: 3-bromopropyl benzene reacts with strong base of potassium tertiary butoxide to give allyl benzene.…

Q: Draw the structure(s) of the major organic product(s) of the following reaction. aqueous H,SO. KCN

A: The reaction given is,

Q: QUESTION 3 Use Hammond's postulate to determine which alkene in each pair would be expected to form…

A: The correct option are as follows:

Q: 46. In order to determine the ident ity of an alkene, a chemist reacts it with water. She then…

A: Organic reaction mechanisms:   As per our guideline we have to answer first question only.

Q: Draw the structure(s) of the major organic product(s) of the following reaction. fuming HNO,

A: HNO3 is a strong oxidizing agent can oxidises the aldehydes When fuming nitric acid (HNO3) react…

Q: Organic chemistry homework help?

A: (A) Methyl carbanion consists of three hydrogen atoms and a lone pair around the carbon atom bearing…

Q: ng carbocations

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Q: Draw the structure(s) of the major organic product(s) of the following reaction CH,0 OCH, "osH…

A: Ketone is formed as a major product.

Q: Consider the following alkyl iodides and identify the most reactive and the least reactive compound…

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

Q: Draw structures of compounds A to D. Br2 2 eq. KOH in ethanol Compound A (C,H12) Compound B Compound…

A:

Q: Draw the structure(s) of the major organic product(s) of the following reaction. aqueous HC

A:

Q: What will the formula be of the main produc

A: Answer is there is formation of ether  CH3OCH2CH2CH3

Q: Explain why the addition of HBr to alkenes A and C is regioselective, forming addition products B…

A:

Q: Question 26 of 42 CH3 CH3 CH3 CH2=CCH,CHCH,OH H2S04, H;C H3C Referring to the above reaction: 1.…

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Q: Why is 5-octene not possible? 2. Why is 3,3-dimethyl-3-octene not possible?

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Q: the structure of compound e.

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Q: Explain the substitution reactions below

A: In this questions, we will explained the substitution reactions for all three given reactions.  You…

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.