2 Indicate which carbocation is the most stable carbocation and which carbocation is the least stable carbocation? H. CH3 CH3 CH3 H. H `H CH3 H3C CH3 II IV %3D
Q: What is the jor product of the following rencfon? CH-CH OH + excess HBr CH-CH Br CH=CH2 b) CH-CHOH…
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Q: CH; +CH CH; I II III IV
A: We have to rank the following given carbocation in order of increasing stability as follows in step…
Q: 4. Draw all resonance structures for the carbocation formed by ortho attack of the electrophile…
A: Concept is based on resonance.
Q: (1) Which is the most stable carbocation? ( H A. CH3-C-CH3 B. CH3-C-CH-CH3 C. CH3-CH-CH3 ČH3…
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Q: Which structure is the most likely product of the reaction below? CHCI3, KOH -CI CI -CI -CI
A: CHCl3 form carbene with KOH then addition of carbene to double bond occur. ->Carbene added from…
Q: Which alkyl halide will form.the most stable carbocation? Br Br Br II II IV Multiple Choice II IV
A: A carbocation is an ion with a positively charged carbon atom.
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: Organic Chemistry Indicate which carbocation is the most stable carbocation and which carbocation is…
A: Carbocation :- Ion with positive charge on carbon atom is called carbocation. The presence of…
Q: Rank the following carbocations in order of increasing stability. CH2 CH3 CH3
A: The carbocation is basically a trivalent carbon whose hybridization is sp2. The higher the…
Q: Rank the following alkenes in order of increasing stability: CH,=C(CH3)CH,CH3, CH2=CHCH(CH3)2, and…
A: Stability of alkene is directly proportional to number of hyperconjugation structures and number of…
Q: CH3 (S) КОН CH3 What is the most likely product of this reaction? CH3 CH3 A H3C H;C H3C CH3 Но CH3…
A: There KOH base is used and this base is strong base but here medium is not mention so that we will…
Q: Which compound is the dominant product in the reaction shown below? Br2 Br (A) (B) Br hv Br (C) (D)…
A: A photochemical reaction is a chemical reaction in which light energy is absorbed by a substance's…
Q: What is the product of the following reaction? `NH2 H,SO, NABH;CN NHCH;CH3 NCH,CH3 HO NHCH2CH3 II…
A: this is an example of reductive amination reaction
Q: Select the correct reagent for the following transformation* ?? CH3CH2CHCH3COCI/Alcl3 O…
A: Benzene is an aromatic compound that is planar, cyclic, conjugation of pi-electrons and, obeys…
Q: Which reagents would you choose to complete the following conversion? Step step and finally step Br…
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Q: Arrange the following carbocations based on their stability. Least Stable 1 2 3 A H₂C Most Stable y…
A: In the Chair conformation , when the bulky substituent is present at the axial position then this…
Q: Which carbocation is the least stable? CH3 lo IV. CH;CCH2 I CH;CH2 II. CH3CHCH3 CH3 CH3 I CH3CO V.…
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Q: CH3 5. Cl-CH,-C –CH2 – CH2 – Cl +I - product; Major product of this reaction is: DMF CH3 CH3 CH3 (а)…
A: In Sn2 reaction, nucleophile attacks leaving group containing carbon, so that leaving group…
Q: 7. Determine the major product of the reaction. CH3 CH3-CH=ċ-CH, + HBr a) CH3 b) CH3 CH,Br-CH=ċ-CH3…
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Q: Arrange the following carbocations in their correct order of stability. 1=Most stable and 4=least…
A: Hyperconjugation is a concept which explains the interactions of the electrons in sigma-bond…
Q: The major product of the following reaction is: CH;CH,S¯ Na CH;CHCH,CH,Br DMSO CH3 CH;CHCH=CH, CH3…
A: Nucleophilic substitution reaction is a class of organic reactions where one nucleophile replaces…
Q: uestion 4 Select the major product of the reaction below. CH3 CH3 CH3 Br B C(CH3)3 C(CH3)3 CH,O Na*…
A: The answer is given as follows
Q: Which alcohol will form the most stable carbocation? CH3 a) CH,CHCH,OH CH3 b) CH—сон CH3 c) -OH d)…
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Q: Determine the reagents required to convert (CH3)2C=CHCOCH3 to each product. [1) [1] 1] Li (1] Br…
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Q: Which will give the most effective yield of ether? CH3CH20 + CH3-CH-CH2BR CH3 PhO- + CH3-CH-Br CH3…
A: Synthesis of ether by Williamson Ether Synthesis.
Q: Which of the following represents allylic carbocation? CH2 - CH = CH, CH3 - CH = C - CH3 CH3 - CH-…
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Q: Rank the following carbocations in decreasing order of stability. (CH3)½C-CHCH2 CH;CH CHCH,…
A: The decreasing order of stability of the carbocations are
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: Na, NH3 5. What is the product of the following reaction? H,CC=CCH,CH,CH(CH,), H,CC=CCH,CH,CH(CH,),…
A: Alkyne in the presnece of Na and NH3 undergo reduction leading to gives trans product by electron…
Q: What product would result from the reaction shown below? CH3 (1) CH3ONA (2) H* (B) (D) (C) CH3 LOCH3…
A: Any molecule or ion which are electron rich species are called nucleophile for example -NH2, -OH and…
Q: What reagents yield the desired product? Br 1) CH3CH2CH2COCI, AICI3 2) Br2, FeBr3 3) NH2NH2, KOH, A…
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Q: 4. In the following examples (where R represents the rest of the molecule), tell which is the best…
A: A leaving group is the one ,which departs with a pair of e- in heterolytic cleavage. A good leaving…
Q: Which has the highest reactivity to Br2/CCI4? I. O,N- II. CHO- -CH=CH2 -CH=CH2 II. IV. H2C- -CH=CH2…
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Q: The major product of the following reaction is: CH;CH2S Na CH;CHCH,CH,Br CH3 DMSO CH;C=CHCH3 CH,…
A: The nucleophilicity of the given thiolate anion (CH3CH2S-) is higher as the polarizibility of sulfur…
Q: Rank the following carbocations from least to most stable: 1 2 O1<3<2 O 2<1< 3 O1<2<3 O 2<3 <1
A: Carbocation stability depends upon the number of alkyl groups attached to it. The alkyl groups have…
Q: "NH2 CH3BR 2H2/Pt H3C-c=CH → A В C
A: Sodium Amide is used as a strong base. The methyl bromide gives the possibility of a nucleophilic…
Q: What are the major products of this reaction? Bre (2R, 3R)-Dibromobutane (2S, 3S)-Dibromobutane (2S,…
A: both 1st and 2nd molecules are major product here
Q: What is the product of the following reaction? F CH;NH2 F NO2 NHCH3 NHCH3 .F .F H3CHN H3CHN H3CHN"…
A: Following is the correct product of the given chemical reaction.
Q: 1) X 2) Y
A: Esterification reaction: Esterification is the process of combining an organic acid(RCOOH) with an…
Q: Rank the following carbocations in order of increasing stability CH3 + + CH3-C CH2-CH3…
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Q: Which reaction provides the best synthesis of 2-methyl-I-butene? (C,Hs);P=CH2 (A) CH3-CH2-C-CH3-…
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Q: Complete the following reactions: KOH a) CH-CH-CH-CHL-Br ) Hg (adela, Hz0 2) Na BH4 b) CH3 - CH2- CH…
A: We have given the organic reaction and we have to complete the reactions.
Q: What is the major product of the reaction sequence below? (1) CH2=CHTMgBr/ether (2) dil. H+/H,0 (3)…
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Q: What reagents are needed to carry out the conversion shown? HO HO 1 mole / H2SO4 2 moles /H30* O…
A: The reaction taking place is given as,
Q: 15. Which of the following carbocations is the most stable? a) ethyl carbocation, CH;CH2* b)…
A: A carbocation is a planar molecule in which a carbon atom has a positive charge and three bonds.
Q: predict the major product of the reaction sequence below
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Q: Which alkyl halide will form the most stable carbocation? Br Br Br Br II III IV Multiple Choice II
A: Carbocation will more More the hyperconjugative structure more
Q: Which one is the product of the following reaction? CH3 CH3 Cat. H2SO, HO ČH3 A а) CH3 HO CH3 ČH3 b)…
A: The above given reaction is a well known example of synthesis of alkene by using alcohol as raw…
Q: 15. CH3 CH3C=CHCH3 + HBr What is the major product for the reaction above? CH3 a. CH;CH-CHCH3 Br CH3…
A: Alkenes are the organic compounds which contains at least one double bond in it. The given compound…
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- For each reaction, decide whether substitution or elimination (or both) is possible, andpredict the products you expect. Label the major products. chlorocyclohexane + NaOC(CH3)3 in (CH3)3COH1. Which among these would be the most stable carbocation?a. Allylicb. Vinylicc. Primaryd. Secondary2. What is the primary reason for the stability of tertiary carbocations?a. Free rotationb. Resonancec. HyperconjugationClassify the following carbocations as 1o, 2o, or 3o and b) rank the following carbocations in order of stability. (1 = most stable).
- Which carbocation is more stable?H2C=C+H OR HC=C+ b HC= C+ OR CH3C+H2When 2-bromo-3-phenylbutane is treated with sodium methoxide, two alkenes result (by E2 elimination). The Zaitsevproduct predominates.(a) Draw the reaction, showing the major and minor products.(b) When one pure stereoisomer of 2-bromo-3-phenylbutane reacts, one pure stereoisomer of the major product results.For example, when (2R,3R)-2-bromo-3-phenylbutane reacts, the product is the stereoisomer with the methyl groups cis.Use your models to draw a Newman projection of the transition state to show why this stereospecificity is observedWhen 2-bromo-3-phenylbutane is treated with sodium methoxide, two alkenes result (by E2 elimination). The Zaitsevproduct predominates.(a) Draw the reaction, showing the major and minor products.(b) When one pure stereoisomer of 2-bromo-3-phenylbutane reacts, one pure stereoisomer of the major product results.For example, when (2R,3R)-2-bromo-3-phenylbutane reacts, the product is the stereoisomer with the methyl groups cis.Use your models to draw a Newman projection of the transition state to show why this stereospecificity is observed.(c) Use a Newman projection of the transition state to predict the major product of elimination of (2S,3R)-2-bromo-3-phenylbutane