The most stable structure of trans-1-Bromo-3-methylcyclohexane is CH3 Br ZCH3 Br. ČH3 Br ČH3 Br

Q: Draw the products, including their configurations, obtained from the reaction of 1-ethylcyclohexene…

A: Since you are asked for multiple sub-parts, we are entitled to solve first three questions.

Q: The most stable structure of trans-1-Bromo-3-methylcyclohexane is ICH3 Br. Br. ČH3 Br CH3 Br

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Q: Name the following dienes and rank them from most stable to least stable. (Hint: Alkyl groups…

A: Naming Rule : Select the longest parent chain keeping both the double bonds in it. And number it in…

Q: (CH3)3C- (CHa)3C Br Br cis-1-bromo-4-tert-butylcyclohexane trans-1-bromo-4-tert-butylcyclohexane a.…

A: Hello. Since your question has multiple sub-parts, we will solve the first three sub-parts for you.…

Q: 2 Indicate which carbocation is the most stable carbocation and which carbocation is the least…

A: Stability of carbocations: more the hyperconjugation, higher will be the stability of carbocations.…

Q: Which two compounds ionize with loss of bromide ion to form the same carbocation? CH3 CH3 CH3 CH2…

A: Halogen which is in conjugation with alkene give carbocation..

Q: Arrange the three alkene isomers in order of increasing stability (least stable to most stable). X…

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Q: What is the best name for the following molecule: H3C. CH3 H3C O4-cyclopentyl-4-methylpent-2-yne…

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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: 1)) Determine the structure of the products in the three reactions and indicate if the final product…

A: HNO3 - H2SO4 is a nitrating mixture that undergoes nitration in benzene.  KMnO4 is an oxidizing…

Q: 5. The following are the structures of fouf a-0-CH,CH-NCHb -o-CH,CH-CHy CH CH2 HC CH- -CH2 HC C-0 CH…

A: (a) The given structure A contains a phosphate group that has a polar end and hydrophilic in nature,…

Q: What stereoisomers are obtained from the following reactions? a. 1-butene + H2O + H2SO4 b.…

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

Q: dy Br Br 3-bromo-4 chlarahexane (Z-3,4-dimethylher-3-ene iv.

A: Given that : We have to give the IUPAC name of the following compounds : and draw the following…

Q: What is the structure of (15.2R)-1-ethyl-2-methyl-1,2-epoxycyclohexane %3D II IV

A: The R, and S configuration of a molecule can be determined on the basis of the Chan-Ingold-Prelog…

Q: The following compound on flipping results in: A trans-1,4-dimethylcyclohexane (a,a) B…

A: There  is a concept of ring flipping.On flipping the axial bond become equotorial and equatorial…

Q: 3(R),4(R) 3-Bromo-3,4-dimethylhexane CH2CH3 Br -CH3 NaOCH3 in CH3OH heat -CH3 CH2CH3

A: There are 3 products possible from the elimination reaction of 3(R),4(R) 3-bromo-3,4-dimethylhexane.…

Q: hich of the following structures represent trans-1,4-dimethylcyclohexane H A CH3 B CH3 C CH3 H CH3…

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Q: Draw a structural formula for the most stable carbocation with each molecular formula. Q.) C4H9+

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Q: What structure below corresponds to 2-methyl-2-hexene? OA. (CH3)2C=CHCH2CH2CH2CH3 OB. CH3 O D. C:…

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Q: Which of the following conformations of 1,2-dibromocyclohexane is the LEAST stable? Select one: Br H…

A: 1st:-  both bromines are trans at 180 degree so there are no any interaction with lone pair-lone…

Q: Which of the followings is the most stable alkene? CH3CH2C=CH2 b. CH3-CHCH=CH2 а. CH3 CH3 CH3CH2 CH3…

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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: O CH2 CH, CH, CH;-CH-CH, CH3-CH-CH,-CH2 CH=CH, CH, CH,-CH-CH-CH, II II IV V.

A: I is a primary carbocation. It is stabilized by +I effect of one alkyl group and 1 hyperconjugable…

Q: Name the following alkenes: (а) CH3 (b) CH3 CH2CH3 (c) CH;CHCH,CH,CH CHCH,CH3 C=C H3C CH3 C=C H3C H…

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Q: 3-hexyne + 1 mole of Br2 → (c) CH3CH2CECCH2CH3 + H2O/H2SO4 → (d) stable structure

A: Alkyne in the presece of Br2 give addition reaction and in the presence of H2O / H2SO4 give…

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

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Q: Which of these two structures is more stable? Provide a brief explanation for your chc :0: :0:…

A: The ions are the charged particles. Whenever an atom loses or gains electrons, it results in the…

Q: The highest energy and be not stable of the following carbocations is: CH2 CH3 CH3 CH3 I II III IV…

A: The carbon atom bearing positive charge is known as carbocation.

Q: 1 Classify the following halides and carbocations as 1°, 2°, or 3°. a) d) h) b) Br Br i) f) c) j) g)

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Q: 10. Identify the higher energy and lower energy forms of two substituted cyclohexanes, for example…

A: The stability of molecules is inversely proportional to the energy of the molecules. This is because…

Q: CH2CH3 OH H3C. to zig-zag (line) notation (include stereochemistry) Br H a) OH HO" to Newman…

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Q: .Br CH3 CH3 1S,2S)-1-bromo-1,2-dimethylcyclohexane Rx de B- Eliminación CH 1,2-dimethylcyclohex-1…

A: β-Elimination is a chemical reaction where atoms or groups are lost from adjacent atoms and it…

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: 16. Which of the following is the most stable carbocation? a) *CH3 b) CH;CH2* c) (CH;),CH* d)…

A: Correct option is - (d) (CH3)3C+

Q: 2-propan-2-yloxypropane H- CH3 -OCH2CH2CH3 CH3CH2CHSH 6. 4. 5. OH CHз SH CH3 LOCH3 CH,CCH2CHCH2CHCH3…

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Q: Which one of the following alkenes is the most stable? H3C CH3 H3C CH3 H3C CH2-CH3 ÇH3 C= H3C. CH2…

A: More substituted alkenes are more stbale.More substituted  alkenes can attain more hyperconjugation…

Q: 18. Of the following structures the most stable carbocation is: a. I b. II c. IV d. III e. I y…

A: In this question, we will Identify the most stable carbocation.  You can see details explanation…

Q: a,2,3,3-tetramethylbutane + Oz $lame. b) u,5-dimethyl cyclohexene thnOx/Ha50x, ) 3-metyl_l-butene…

A: Depending on the difference in reaction condition the different type of product is formed .

Q: The products created when 1-methylcyclopentene reacts with one equivalence hydrogen bromide are: H3C…

A: Alkene gives an electrophilic addition reaction with hydrogen halide. The reaction proceeds in two…

Q: TRUE OR FALSE i. A =C-Br bond is more polar than a -C-Br bond. ii. A bromonium ion can undergo…

A: We have to tell the given statements are true or false. The given statements are A =C-Br bond is…

Q: 1. Arrange each set in order of decreasing priority using (Cahn-Ingold-Prelog) priority rules…

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Q: (b) 1-methyl -3-chloro-4-lodo Cyclo pentane (C) 1- Chloro-2-lodo-4-methyl Cyclo pentane (d)…

A: The question is  based on concept of IUPAC NAMING of organic compounds. There are certain rules to…

Q: Which of the following is the most stable alkene 1. 2 H,C HC H,C. HC. CH3 CH CH, A. two of these…

A: As the substituents (alkyl groups) on alkene incrases stability of alkene increases

Q: 3,4-dimethylpent-2-ene A₂

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Q: Which of the following carbocations is the least stable? -CH2* O (CH3)3C* O (CH3)2CH+ O CH2=CHCH,+

A: Carbocation: carbon ion that bears a positive charge on it.

Q: 4. Br Br Br -CI Br - CI H3C H3C H3C CH3 C Which of these is a Fischer projection of (S)…

A: (S)1-bromo-1-chloro-1-fluoropropane

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

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Q: Which of the following carbocations would you expect to rearrange?

A: A chemical reaction mechanism represents the way to form and break the chemical bonds between…

Polymerization Kinetics

Polymerization is a chemical process in which one or more monomers combine to produce a very large chain-like molecule called a polymer. The functional groups present on the monomers and their steric effects are responsible for polymerization through a sequence of reactions that diverge in complexity. There exists a stable covalent chemical bond between monomers that sets apart polymerization from other processes. Polymerization is generally classified into step-growth and chain polymerization. Polymers are categorized into linear polymer and cross-linked polymers that are produced either by condensation or additional polymerization.