1. KMNO4, HO, Hа0, heat CH3 2. HС H,C- Product 2 ČH3

Q: t. uänoJu su view structure Part 2 out of 2 Why would this be a more stable carbocation? The charge…

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Q: Rank the following groups of alkenes from least stable (4) to most stable (1)

A: Interpretation- To tell about the stability order of alkene in above given question and then in…

Q: A terminal alkyne (RC=CH) is exposed to excess HBr. What rule should be followed to determine the…

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Q: Which reaction is not stereospecific? Br,/CCI, trans-2-butene Br,/H2O cis-2-pentene II HBr…

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Q: What are products formed from the below reaction? Draw the stereoisomers and name them. (Hint: There…

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Q: Addition of HBr to allene (CH2=C=CH2) forms 2-bromoprop-1-ene ratherthan 3-bromoprop-1-ene, even…

A: In allene, centre carbon is sp hybridized. The electronegative nature increases with increase in…

Q: What alkenes are formed from each alkyl halide by an E1 reaction? Use the Zaitsev rule to predict…

A: E1 reactions: These reactions proceed in two parts. Lose of leaving group. Removal of proton These…

Q: 4. (2 pts) Circle the most stable carbocation and cross out the least stable carbocation among the…

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Q: Question attached

A: Applying concept of organic synthesis and reagent.

Q: What is the major final product of the following reaction sequence? Only ane enantiomer of the…

A: The possible product has to shown

Q: Identify the least stable carbocation. O CH3* +. O *CH2CH3 O (CH3)3C* O (CH3)2HC*

A: The stability of carbocation depends on the electron donation effect of the groups attached to the…

Q: If a mixture of products is expected, the more stable alkene is the major product. Recall that the…

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Q: Draw all possible constitutional isomers formed by dehydrohalogenation of each alkyl halide. Br CH3…

A: Since we only answer up to 3 sub-parts, we’ll answer the first 3. Please resubmit the question and…

Q: What is the major monobromination product formed by heating each alkane with Br2? b.…

A: Since you have posted a question with multiple sub-parts, we will solve first three subparts for…

Q: Draw the product or products of the reaction. Include charges where appropriate. Draw the…

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Q: In each box, provide either the missing reagents or the major organic product for each reaction…

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Q: C.

A: Tertiary (3°) carbonation is more stable than secondary (2° ) because 3° carbonation is more…

Q: Cuando se añade H-Br a un alqueno terminal el producto sigue la regla de Markovnikov. O a. Cierto O…

A: Note: According to our guidelines we are supposed to answer only one question.  Kindly repost other…

Q: Question 8 Rank the following carbocations from most stable to least stable: II II O III >I> II OI>…

A: Given that, Three carbocations have been given,we have to find out order of stability?

Q: (CH3)3CHOH is reacted with CH3-O-C--C6H5 in a transesterification reaction.  What is the M+ of the…

A: Given reaction is trans esterification reaction.

Q: Peroxides) CH3 CH3 (b) CHCH3 HI ? (a) HBr CH3CH2C=CHCHCH3

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Q: Encircle the most stable alkene. CH3 CH3 CH3 a) CH3 CH2CH3 b)

A: A question about the stability of alkene, which is to be accomplished.

Q: Which of the following represents allylic carbocation? CH2 - CH = CH, CH3 - CH = C - CH3 CH3 - CH-…

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Q: 2. Please give the order of reactivity of alkenes CH3-C=ç-CH3 CH; CH3 CH3-C=CH-CH3 CH3-CH=CH-H CH3 B…

A: With the increase in the number of alkyl groups attached to the double bonded carbons, electron…

Q: Which pair of reactants is most likely to undergo an E2 reaction? O CH3SH + CH3CH₂CBr(CH3)2 at 20°C…

A: The given problem is based on the chemical properties of alkyl halides.

Q: 1. As we've seen, SN1/E1 reactions can be quite messy and can generate multiple products. Consider…

A: Alkyl halide gives elimination and substitution reactions. Both E1 and SN1 reactions proceed by the…

Q: CH2 NBS , CCI4 heat CH3 CH2Br CH3 CH2 CH3 CH,Br Br Br Br Br

A: Allylic position is that position which is next to double bond.

Q: a) CH3 b) CH3 – CH – CH- CH3 CH3 с) СНЗ — СН2 —- CH - СHЗ

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Q: Br HBr CH3-C=C-H CH3-C=CH2 The previous equation for one of the reactions of alkenes, and explains…

A: The answer to the following question is-

Q: Draw the structure of the product of the reaction between the compound shown below and H,SO,…

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Q: When this alkene is subjected to the conditions shown, two equivalents of a single product is…

A: Let's find the product of the given reaction in the question which is 2 equivalent.

Q: Draw the intermediate carbocation that is formed when each is protonated, say, with H+.These occur…

A: We know that when we add HX like HBr , HI ,HCl or H+/H2O we first get carbocation then the…

Q: Addition of HBr to allene (CH2=C=CH2) forms 2-bromoprop-1-ene rather than 3-bromoprop-1-ene, even…

A: In any compound, carbon that possesses sp3-hybridization and carries +ve charge is stated as…

Q: Complete the diagram by drawing a Newman projection of the product of this reaction in its most…

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Q: Draw the starting alkene that would lead to this the major product (and its enantiomer) under these…

A: Catalytic hydrogenation is a process in which treatment with H2 in the presence of catalyst like Ni,…

Q: ify the major organic product generated from the reaction shown. : D = a deuterium atom, which…

A: Alkenes are organic compounds that contain double bond between carbon atoms.

Q: + 1. Draw line structures of all of the C3H17* carbocations that have the carbon skeleton shown…

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Q: Он PCI, НО b) CI CI CHCI3 NaOH c) HBr excess

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Q: How many of the following will undergo a favourable rearrangement to a lower energy carbocation? H3C…

A: We know the stability of carbonation is tertiary> secondary> primary.Again if a carbonation…

Q: This Diekmann cyclization proceeds through the expected five-membered ring transition state. Draw…

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

Q: 6. Draw the reagent that converts the alkene below to the epoxide (oxirane) c=CH2 CH2 H,CH,C°…

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Q: What are the products of this NBS bromination reaction? CD2=CH-CH3 + N-Br hv (A) CHD=CD-CH,-Br and…

A: The answer is given as follows

Q: In the elimination of a vicinal dihalide to yield an internal alkyne, two equivalents of NaNH, are…

A: The hydrogen atom bonded to triple bonded carbon atom in alkyne is acidic hydrogen and can be…

Q: 2 3 4

A: STRUCTURE having more number of hyoerconjugable H are most stable . ALPHA H are those Hydrogens…

Q: Draw the products of the attached reaction, including stereochemistry.

A: During Bromination of alkenes, the π-elcetrons of the alkene attack the Br2 from downward position…

Q: .CH3 H3C `CH3

A: Electrophilic addition reactions are those reactions in which an electrophile is attacked by a…

Q: Match each alkene to its heat of hydrogenation. Alkenes: 3-methylbut-1-ene, 2-methylbut-1-ene,…

A: The structures of given compound are shown below:

Q: In the elimination of a vicinal dihalide to yield an internal alkyne, two equivalents of NANH2 are…

A: Elimination of vicinal dihalide to yield an alkyne,two equivalents of NaNH2 are required to…

Q: Rank the following carbocations from most stable to least stable:

A: Since more is the resonance of +ve charge on Carbon, more it will be delocalised. Hence more will be…

Q: Addition of HBr to allene (CH2 = C = CH2) forms 2-bromoprop-1-ene rather than 3-bromoprop-1-ene,…

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Alkanes and Cycloalkanes

Alkanes are saturated organic compounds which are made up of C and H atoms. Alkanes have the general formula of CnH2n+2. Alkane contains sp3 hybridized carbon atoms with four sigmas (σ) bonds & every hydrogen atom is connected with one of the carbon atoms. The size of the alkane could be determined by the number of carbon atoms located in it.