Identify possible product(s) of dehydrohalogenation of cis-1-bromo2-methylcyclohexane. кон ELOH Br CH3 H H CH3 only CH3 CH3 CH3 only CH3 CH2

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 shown below? Click on a letter A to D to answer. CH, CH3…

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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: 17. Which of the following is the most stable alkene? a) CH2=CH2 b) CH;CH=CH2 c) CH;CH=CHCH; d)…

A: The answer is given as follows

Q: Identify compound Y? Ha Br2 CH3=-CH3 Y Lindlar Pd O 2-bromobutane meso-2,3-dibromobutane racemic…

A: We have to predict the product Y.

Q: Which le the best synthesia of cyclopentyl ethyl other? a) • CH-CH-OH H. heat ONa H* b) + CH2-CH2 H,…

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Q: What is the proper relationship of the substituents for the major product (only) of the following…

A: In the given structure amide group is present in the ring. We know amide group is ortho/ para…

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

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Q: 6. From what alkyl halides are the following alkenes have been made? CH3 CH3 CH3CHCH2CH2ĊHCH=CH2 7.…

A: Dear student, Bartleby platform allow us to only first question. So please repost the other question…

Q: A student adds NBS to a solution of 1-methylcyclohexene and irradiates the mixture with a sunlamp…

A: INTRODUCTION: NBS is N-bromo succinimide which is considered as a source of bromine Free radical in…

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: Rank the following carbocations in order of increasing stability. + CH,CH,CH2CH2CH=CH b.…

A: To rank the given carbocation in the order of increasing stability.

Q: 3Which of the following alkyl radicals is the most stable? O A. OB. C. OD. O . CH3 CH2. CH3 CH3 CH3…

A: the stability of the radicals are in the following manner. tertiary radicals > secondary radicals…

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

A: Most stable  structure  trans -1 bromo -3-methyl cyclohexane  on the basis of angel strain energy.

Q: 56. Compound X (C;H12) is hydrogenated in the presence of Pd/BASO4 to produce (Z)-2-methyl-…

A: Alkynes on treatment with H2 and Pd/BaSO4 produces cis alkene. A compound containing two or more…

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: Problem attached

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

Q: Determine the product(s) formed when cyclohexene is treated with the following reagents. Br HO. HO…

A: Dear student since it is a multiple type questions with multiple subparts so according to Guidlines…

Q: C\ Rearrangement the following structures by increasing melting point? CH3 CH3 ОН D\ Rearrangement…

A: With increasing in molecular weight,  both melting point and boiling point increases.  H- bonding is…

Q: For the following five reactions, draw the product(s) obtained from the cycloalkene and the reactant…

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Q: What is the major organic product of the reaction shown? CH3C=C: Br A. 5-methylhex-2-yne OB.…

A: Nucleophilic substitution biomolecular reaction (SN2): The bimolecular nucleophilic substitution…

Q: Products of the following reaction CH3 - CH = C– CH2 – CH3 (1) O2/ ether (i)Zn/H2O CH3 are CH; – CH+…

A: Introduction: Alkene gives electrophilic addition. Ozonolysis is a reaction in which alkene reacts…

Q: Which alkene is the main product of acid-catalyzed dehydration of 3-methylbutan-1-ol? Оа. Н CH3 c=C…

A: Acid catalyzed dehydration reaction is a type of reaction in which an organic compound, alcohol in…

Q: Which of the following reagents would NOT convert the starting material to the shown product? ??? OH…

A: c

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: 5. What is the IUPAC name of the major product for the reaction shown in the box? NaN3 ? DMSO `CH3 O…

A: Given reaction follows SN2 mechanism.  That means nucleophile attacks from backside of leaving…

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 represents allylic carbocation? CH2 - CH = CH, CH3 - CH = C - CH3 CH3 - CH-…

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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: Identify the secondary carbocation from the following: o (CH3),CHCH2* O CH3CH2* o (CH3),CH* O CH3*

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Q: For each reaction, decide whether substitution or elimination (or both) is possible, andpredict the…

A: Bulky bases prefer elimination whereas non-bulky bases prefer substitution reaction.

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: Fill in the product, starting material, or reagent for each reaction. "No reaction" is a…

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Q: I need help with both drawing and labeling these problems!

A: Name of the given compounds:(E) 1e-[2-Ethylpentyl]-2a-ethylcyclohexane    and    (F)…

Q: 12. Which one of the following is INCORRECT transformation? SOCI, NH2 三V 三V MeMgBr, THF, then H3O b)…

A: In the given reactions to find out the incorrect transformation.

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: (S)-3-methyl-1-penten-4-yne; f. (3S,8S)-8-chloro-3,8-dimethyl-5-decyn-3-ol e. g.…

A: Structure of given compounds can be drawn by following IUPAC nomenclature rules.

Q: Which of these alkenes would react most slowly with HCI? CH3 (CH3),C=C CH,CH3 O CH;CHCH=CH2 CH3 ©…

A: The addition of HCl to alkene is an example of electrophilic addition reaction. The rate of this…

Q: PQ-11. What compound is the least likely product of the reaction of 1,3-butadiene with HCl? (A)…

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Q: 67. What is the IUPAC name for the following molecule? H. a.…

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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: What is the possible products for following compound with one equivalent of HBr? 3,4…

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Q: Show how to prepare the following cyclopropanes?

A: It is used to synthesise the cyclopropane derivatives.  Cis alkenes give cis- Compounds.  Reagent :…

Q: Q 2(a) Name the following alkenes and rank in order of increasing stability. CH, CH, i) i) CH,…

A: Alkenes is the class of hydrocarbons which contains a carbon-carbon double bond and it is an…

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: Following are   example  of Cope rearrangements of 1,5-dienes. Show that   product can be formed in…

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

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Q: Which reagent can be used to achieve the transformation shown? * C,H5. C,H5. 1.) ? 2.) H,O* CH3 CH,…

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Q: 1. Starting from 1-bromoethane, synthesize ethanenitrile Br CH3CEN 1-bromoethane ethanenitrile

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Reactions of Ethers

Ethers (R-O-R’) are compounds formed by replacing hydrogen atoms of an alcohol (R-OH compound) or a phenol (C6H5OH) by an aryl/ acyl group (functional group after removing single hydrogen from an aromatic ring). In this section, reaction, preparation and behavior of ethers are discussed in the context of organic chemistry.

Epoxides

Epoxides are a special class of cyclic ethers which are an important functional group in organic chemistry and generate reactive centers due to their unusual high reactivity. Due to their high reactivity, epoxides are considered to be toxic and mutagenic.

Williamson Ether Synthesis

An organic reaction in which an organohalide and a deprotonated alcohol forms ether is known as Williamson ether synthesis. Alexander Williamson developed the Williamson ether synthesis in 1850. The formation of ether in this synthesis is an SN2 reaction.