Q: The most stable structure of trans-1-Bromo-3-methylcyclohexane is ICH3 Br. Br. ČH3 Br CH3 Br
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Q: What is the major product of the reaction between 1-chloro-2- methylcyclopentane andsodium hydroxide…
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Q: . Which one of the following is the major product of the reaction of 1-methylcyclohexene with…
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Q: Which two compounds ionize with loss of bromide ion to form the same carbocation? CH3 CH3 CH3 CH2…
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Q: Draw the structure of the four allylic halides formed when 3 methylcyclohexene undergoes allylic…
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Q: Acid-catalyzed dehydration of 3,3-dimethyl-2-butanol gives three alkenes: 2,3-dimethyl-2-butene,…
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Q: Which reaction would you expect to be faster, addition of HCl to 2-methyl-1-butene or to 1-butene?…
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Q: Choose the correct answer on the following questions: Zaitsev’s rule states that: the alkene with…
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Q: Using cis- and trans-hex-3-ene, demonstrate that the addition of HCl is not a stereospecific…
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Q: Using cis- and trans-hex-3-ene, demonstrate that the addition of HCl is not a stereospecic reaction.…
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Q: Reaction of 2-methyl-2-butene (above) with HBr might, in principle, lead to a mixture of two alkyl…
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Q: Reaction of 1-butene (above) with HBr might, in principle, lead to a mixture of two alkyl bromide…
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Q: increasing stability of the double bond
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Q: Rather then forming a carbocation, the addition of Br2 to an alkene generates a ion.
A: The addition of Br2 to an alkene generates a radical ion.
Q: trans-1-bromo-2-methylcyclohexane + sodium methoxide
A: We have given two reaction In first one their is Sodium methoxide present which is strong base than…
Q: The expected Markovnikov addition product of HI to 2-methyl-2-butene is: 2-iodo-1-methylbutane…
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Q: 2. What Alkene would be used to synthesize 3-bromohexane? + HBr CH3CH2CHCH2CH2CH3 Br
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Q: What is the major product of the reaction between 1-chloro-2-methylcyclopentane andsodium hydroxide…
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Q: What five-carbon alkene forms the same product whether it reacts with HBr in the presence of a…
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Q: Match each item to a choice: 1,2-dibromoalkane addition of -OH to the highly substituted carbon of a…
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Q: Which of the following represents allylic carbocation? CH2 - CH = CH, CH3 - CH = C - CH3 CH3 - CH-…
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Q: Rank each group of compounds in order of increasing heat of hydrogenation.(a) hexa-1,2-diene;…
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Q: Draw the major products obtained from the reaction of one equivalent of HCl with the following…
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Q: Acid-catalyzed dehydration of 3,3-dimethyl-2-butanol gives three alkenes: 2,3-dimethyl-2-butene,…
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Q: If you react 1-hexene with hydrochloric acid with peroxides, what product will you produce?
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Q: cis-1-Bromo-4-tert-butylcyclohexane and trans-1-bromo-4-tert-butylcyclohexane both react with sodium…
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Q: Which is not an alkene formed when 2-chloro-2-methylbutane is dehydrohalogenated with NaOCH2CH3…
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Q: For each alkane, which mono brominated derivatives could you form in good yield by free-radical…
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Q: The products created when 1-methylcyclopentene reacts with one equivalence hydrogen bromide are: H3C…
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Q: Identify the type of reaction for the following:1. formation of (S)-2-butanol from (S)-2-bromobutane…
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Q: the reaction of 4-methoxybenzaldehyde and cyclohexanone produces what product? Draw the product…
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Q: Radical bromination of propene using NBS gives 3-bromo-1-propene. Draw the allylic radical…
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Q: What alkyl halide and what alkene would yield the following cyclopropane derivative in the presence…
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Q: Draw the substitution and elimination products for the following reactions, showing the…
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Q: Which is the major product of the reaction if the given structure of 1- cyclopentene reacts with…
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- draw the two possible carbocations that can form when this alkene reacts with a strong acid (such as HBr or H3O+). of the two structures you drew, circle the more stable carbocationWhat reagents in what order would you use to convert 1,2-dimethylcyclohexane to trans-1,2-dimethyl-1,2-dihydroxycyclohexane?Draw the product that would form when 4-methylcyclohexene reacts with chlorine.
- Which isomer of 1-bromo-3-isopropylcyclohexane reacts faster when refluxed with potassium tert-butoxide, the cis isomer or the trans isomer? Draw the structure of the expected product from the faster-reacting compound.the reaction of 4-methoxybenzaldehyde and cyclohexanone produces what product? Draw the product what is the molecular formula of the product how many degrees of unsaturation are present in the productDraw the carbocation you'd expect from the reaction of 2-chloro-3-methylbutane with AlCl3?
- Reaction of 2-methyl-2-butene (above) with HBr might, in principle, lead to a mixture of two alkyl bromide addition products. Draw these two alkyl bromides.Draw the product or products that will be obtained from the reaction of cis-2-butene and trans-2-butene with each of the following reagents. If a product can exist as stereoisomers, show which stereoisomers are formed. 1. HCl. 4.Br2 in CH2Cl2 7. H2O + H2SO4 2. BH3/THF, followed by HO-, H2O2, H2O 5. Br2 + H2O 8. CH3OH + H2SO4 3. a peroxyacid 6. H2 + Pd/CIdentify two alkenes that react with HBr to form 1-bromo-1-methylcyclohexane without undergoing a carbocation rearrangement.
- What effect, if any, do you expect the three different substituents on the aromatic ring (para-chloro, para-methoxy, para-methyl) to have on the reaction? Explain.For each of the following reactions, draw the major elimination product; if the product can exist as stereoisomers, indicate which stereoisomer is obtained in greater yield. a. (R)-2-bromohexane + high concentration of CH3O- b. (R)-3-bromo-3-methylhexane + CH3OH c. trans-1-chloro-2-methylcyclohexane + high concentration of CH3O- d. trans-1-chloro-3-methylcyclohexane + high concentration of CH3O- e. 3-bromo-3-methylpentane + high concentration of CH3CH2O- f. 3-bromo-3-methylpentane + CH3CH2OHWhat is the final product if cyclohexene is made to react with Br2 followed by treatment of a strong base? 1,2-dibromocyclohexene cyclohexyne 1,3-cyclohexandiol 1,3-cyclohexadiene