Which of the following alkene will form the most stable carbocation when reacts with HBr? Select one a cyclohexene b 2 heptene Ci methyleyclohexene. 1-nonane

Q: . Which one of the following is the major product of the reaction of 1-methylcyclohexene with…

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Q: Rank the following alkyl halides according to SN2 reactivity. Put the most reactive compound at the…

A: To rank the given alkyl halides according to Sn2 reactivity.

Q: Draw the structure of an eight-carbon alkene that would yield the following compound (and no others)…

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Q: Identify the most stable carbocation. Select one: О . ОН

A: We have given the organic compound having alcohol as functional group we have to identify the most…

Q: 6) Which of the following best describes the geometry about the carbon-carbon double bond in the…

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Q: When 2-bromo-2,3-dimethylbutane reacts with a strong base, two alkenes (2,3-dimethyl-1-butene and…

A: An E2 reaction is a concerted, one-step reaction in which the proton and the halide ion are removed…

Q: Which alkyl halides can be prepared in good yield by radical halogenation of an alkane?

A: Alkanes undergo both bromination and chlorination. But Chlorination happens faster than bromination…

Q: What is the expected product from the addition reaction of 1-pentene (CH₂=CHCH₂CH₂CH₂) with bromine…

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Q: Halogenation of alkenes will form alkyl halides with 1 halogen substituent O True O False

A: Please find your solution below : The reaction of halogenation of alkenes, most commonly bromination…

Q: Identity the carbocation that is the most stable? a. CH2CH3 CH O b. CHCH, CH, с. CH d. CH,CH2 CH;

A: Carbocation is species in which carbon is carrying positive charge on carbon. In carbocation, carbon…

Q: 5. a) Determine the major product that is formed when the alkyl halide reacts with a hydroxide ion…

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Q: či C-CH2- CH3 CH3

A: Bulky base like EtO- , or alcoholic KOH , generally well known for elimination . elimination…

Q: Which of the following alkenes is the most stable? O O

A: Alkenes are compounds having double-bond. The stability of alkene is determined by the number of…

Q: What will be the product for the given reaction? CH2 = CHC ≡ CH + HCl →? vinylacetylene a)…

A: Alkyne group having two pi-bond is more reactive towards the electrophilic attack than alkene with…

Q: Bromine adds to cis- and trans-2-butene to give different diastereomers of 2,3-dibromobutane. What…

A: According to the question, we get that bromine adds to cis- and trans-2-butene to give different…

Q: In the reaction given below, what type of reaction is used? * KOH Minor Major (cis + trans)…

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Q: Name of the following alkenes with their E/Z confiquration Br %3! Hg C CH9 2) CI 3) CHS TH3

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Q: Which of the following alkenes will yield a meso dihalide when reacted with Br/CCh at room…

A: Alkene reacts with bromine to form dibromoalkane. The reaction proceeds by the bromonium ion…

Q: (1) Predict the outcome of the addition of HBr to (a) trans-2-pentene, (b) 2-methyl-2-butene, and…

A: As far the policy of the company only  first question can be answered at a time. please re-post the…

Q: Which of the following carbocations would rearrange after reaction with HX? a. Хон b. ҳ CA ОН 'OH

A: -> When alcohol reacts with hydrogen halide Reaction proceeds through formation of carbocation…

Q: 1. Reaction of 2,3-dimethyl-1-butene with HBr leads to an alkyl bromide, C6H13Br. On treatment of…

A: We’ll answer the first question since the exact one wasn’t specified. Please submit a new question…

Q: What is the major product of the reaction when the alkane reacts with Cl2 instead of with Br2?…

A: Given: The given alkane reacts with Cl2 instead of Br2.

Q: Which reagent below would be used to convert the following alkyne to the alkene shown? محمو NaNH2,…

A: -> Alkyne can be reduced to trans alkene in presence of sodium/ liq NH3 .

Q: Which of the following alkenes releases the least heat per mole upon hydrogenation? O…

A: The quantity of energy is released when one mole of an alkene is hydrogenated by H2 and converted…

Q: If cis-2-butene is treated with meta-chloroperbenzoic acid what is the final product? Hil Hil CH…

A: Meta perchlorobenzoic acid is also called m-CPBA. It is reagent for epoxidation of alkene.  When…

Q: Which alkene is most stable? Ct2 HC CH3 H2C CH3 CH A

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Q: Addition of HCI to the unsymmetrical alkene below could potentially give rise to two products. C2H5.…

A: Addition of HCl to the unsymmetrical alkene is an electrophilic addition and occurs through…

Q: What alkene should be used to synthesize each of the following alkyl bromides?

A: Since you have submitted multiple subparts, we are solving only first three subparts for you. If you…

Q: CI C=C CI (а) H (b) OH (с) Br

A: (a)  This alkene has cis conformation because higher priority groups are seen on the same sides of…

Q: Assign E or Z stereochemistry to the double bonds in each of the fol- lowing alkenes, and convert…

A: The configuration E is used to describe alkenes where the two highest priority substituents are on…

Q: Addition of HCl to alkene X forms two alkyl halides Y and Z. Label Y and Z as a 1,2-addition product…

A: To find: 1,2 addition and 1,4 addition product of the given reaction

Q: 7a. The reaction below is the chlorination of an alkane. There are four possible mono-chlorinated…

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Q: From which alkene can the following alkyl halides be obtained? Cl CH3 CH,CH3 с) а) CH; - CH, - С -…

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Q: 6. Which of the following alkenes is most reactive in the Heck reaction? in %3D IV A. I B. II C. III…

A: The given structures are represented as follows:

Q: Directions: Write the product of the addition reaction. 1. Addition of HBr to H2C=CH2 2. Addition of…

A: Write the product of the addition reaction.   1. Addition of HBr to H₂C=CH₂ 2. Addition of Br2 to…

Q: Which of the following alkenes is most stable? A) I B) II C) III D) all of them

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Q: What is the major product of the following addition reaction of alkyne? H-Br A B D Br Br Br Br

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Q: What alkene starting material would produce 2,3 -diiodopentane when reacted with molecular iodine…

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Q: Which alkene is the main product of the following reaction? OH Cat. H2SO4 A

A: According to Saytzeff rule, more subsituted alkene is major product.

Q: When 1-butene reacts with HBr the reaction mechanism proceeds through a? secondary carbocation…

A: Reaction of 1-butene with HBr is an addition reaction. The HBr add to double bond as per…

Q: What is the expected product from the addition reaction of excess HBr to 2- butyne? A) 2-bromobutene…

A: Alkyne give addition reaction with HBr and when 2-butyne react with HBr then HBr added across the…

Q: 2 3 4

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

Q: Which alkene is predicted to be the most stable? II II IV

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

Q: Which of the following alkenes will yield a meso dihalide when reacted with Br2/CCI4 at room…

A: Meso compounds are those compound which have more than one stereocenters. They are superimposable.…

Q: Identify the structure of the starting alkene in the following case: CH3 1) O3 2) DMS H3C C3H,4

A: In this question, we have to find out the correct answer of given problem by the help of the…

Q: Which substituent would be assigned the highest priority when naming an alkene E or Z? 0 0 O 0=0 CH₂…

A: The naming of alkene as E or Z is done on the basis of the presence of higher priority groups. When…

Q: Which of the following alkenes do not show cis-trans isomerization? I) 2-methyl-2-hexene II)…

A: Since you have posted multiple questions, we are entitled to answer the first only. 1) The compounds…

Q: Addition of HBr to 1,3-Butadiene produce A- 3-Bromo-1-butene B- 1-Bromo-2-butene C-…

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Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.