Please give a reasonable mechanism for the following reaction using a multiple component reactions. Please draw it out and write out the steps, PLEASE SHOW WITH ARROWS

Q: H E1 ČI

A: Here E1 elimination takes place . Since in E1 elimination carbocation intermediate is formed so…

Q: Provide the major product(s) of the following reaction and the corresponding mechanism.

A: Benzene rings are electron-rich due to the presence of pi  electron density. Hence it can be…

Q: OH H2SO4 HOCH,CH3 Doubling [CH3CH,OH] doubles the rate of rxn.

A: Given : Doubling concentration of CH3CH2OH doubles the rate of reaction.

Q: 0. Br2 H2O НО

A: The given reaction is an example of acid catalysed conversion of epoxide to diol.

Q: ОН heat

A:

Q: In the following electrophilic aromatic substitution reactions, the overall transformation is the…

A: In electrophilic aromatic substitution reaction,  an electrophile is added to aromatic ring and…

Q: For the reaction below, provide a mechanism for the formation of intermediate A and product B. Show…

A: Reaction 1 : 6 pi electrocyclization and dis rotation is favored under thermal conditions. Reaction…

Q: Draw the product and mechanism for the reaction below. Include all major resonance structures.

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Q: (in THF) 2.H dilute

A: In the first step nucleophile CH2- attack on carbonyl carbon and π bond transfer towards more…

Q: ОН Д CO₂H H2O да

A: Alcohols participate in dehydrationTertiary Alcohols readily participate than the primary and…

Q: CN .CN NH3 CH3OH Br Br `NH2

A:

Q: Please answer all of the following neatly clearly and thoroughly! Thanks Consider the given reaction…

A: Le Chatelier’s principles : In reversible reactions When factors like concentration, pressure,…

Q: Draw the mechanism for the following reaction with arrows and include all intermediates. Include…

A: The F-NR2 attacks on the triple bond of the compound and results in the formation of an allene…

Q: Br HI (1 eq.),

A:

Q: Please don't provide handwritten solution ....  do these reactions give identical products, show…

A: Hydroboration is the addition of borane to unsaturated to form alkyl borane. In BH3, hydrogen is…

Q: CH;OH Br +

A: In the given reaction, there are two products formed which are enantiomers of each other. Hence it…

Q: d) synthesize reaction. please show mechanisms if there is any.

A:

Q: Br AgNO3 EtOH

A: This is an example of silver ion mediated SN1 reaction

Q: Q₂N NO ₂ NO2 2 HO" | H₂O 02N 0₂4. NOL

A: Electron withdrawing groups increase the stability of carbanion and make the reaction faster.

Q: Br 'Н 1- excess NaCN, Et₂O-H₂O 2- excess HC1, H₂O - ?

A: Product of following reaction is made by applying appropriate reaction mechanisms.

Q: Br (3)+(3 Br t-BuOK (2 equiv.) t-BuOH, heat

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Q: Progress of reaction Which of the following mechanisms is consistent with the reaction profile shown…

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Q: CH2CH3 H3CH2C- Br CH;OH 1) CH2CH3 CI H2Q 2) H3C-C- CH2CH3 (R) 3) CH;CH,CI NaOCH,CH3 CH3 4) NaOH…

A: SN1 Reactions: Nucleophilic substitution reactions, in which the tertiary or secondary alkyl halide…

Q: C Write a mechanism for the step shown below, using curved arrows to show electron redistribution.…

A: Acetals are the products formed by the reaction between aldehyde or ketone with alcohol. Acetals are…

Q: о || | (b) Me-C-C-Ph ОН ОН Ph (а) Мe— (A) CH- | | OH (d) Ph-C-C-0-Me (c) Me-C-COOH Coin Ph

A: Answer :

Q: Draw the mechanism for Llle Lll աայււմ 11 i) This mechanism requires 6 steps. ii) Make sure you draw…

A: Ester undergoes reaction with alcohol in the presence of acid to form the different ester and…

Q: Br₂, Heat H COOCH, Br + HBr

A:

Q: Consider the reaction below. a) Predict the reaction mechanism that is likely to operate between…

A: The given reaction is an example SN1 reaction stands for substitution nucleophilic unimolecular. The…

Q: alternate route or reaction? I

A: Your proposed reaction scheme is ok. Only one problem is that F being electron withdrawing group,…

Q: Can you show the mechanism? Every steps

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Q: In the problem-solving feature above, methylcyclohexanone was seen to react at itsunsubstituted a…

A: The regiochemistry is not observed has to be explained.

Q: OTs - (strong base) В Doubling [B] doubles rate of rxn.

A: The reaction involves a carbocation intermediate and is commonly seen in reactions of secondary or…

Q: НО ОН OH mCPBA CrO 3, H30+ PCC ? None of the above НО д

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Q: Consider the following overall reaction and proposed mechanism. Evaluate whether each step of the…

A: The proposed mechanism is represented as follows:

Q: HBr Br

A: The mechanism is Addition of HBr via hydride transfer.

Q: 11.5 Propose a reasonable organic reaction mechanism for the reaction shown below using the curved…

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Q: b)Show the mechanism for the steps of the following reaction and how they give the final product.…

A: The details solution for this reaction is provided below in attach image.

Q: oxidation reduction neither Give detailed Solution with explanation needed of all options. don't…

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Q: When an NMR spectrum is taken of the molecule below, there is the expected 5H in the aromatic…

A: 1H-NMR spectra is used to identify the hydrogen environment of the unknown compound which helps in…

Q: Predict the products of the following reactions: (a) NaBH(OAc)3 butan-2-one + diethylamine (c) (e)…

A: We have find out the answer.

Q: b) Suggest the major product of the following reactions and predict the mechanism of each reaction.…

A: Protonation of alkene/alkyne to produce carbocationAddition of Br- to produce product

Q: N MgBr 1. 2. H3O+

A: This is addition of Grignard reagents to nitriles to give ketones after hydrolysis.

Q: Copy the given reaction and show the mechanism by supplying the appropriate curved arrows. Also,…

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Q: Draw a curved arrow mechanism for the substitution reaction that will occur with the alkyl halide…

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Q: p-bromo-toluene Br cyclohexene i. KMnO4, NaOH, heat ii. H3O+ iii. PCI5 iv. NaN3 v. heat vi. H₂O i.…

A: There are two reactions schemes are given. We have to draw the bond line structures of the product…

Q: What is the exact reaction mechanism behind this reaction? I understand how to get from BHA to the…

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Q: Do not use carboxylation mechanism but show full mechanism for the question below

A: Step 1:• Firstly strong base i.e NaOEt abstract the acidic proton to forms enolate anion which…

Q: Provide a complete mechanism for both steps in the reaction, including all lone pairs, formal…

A: The reactant used is a four carbon terminal alkyne i.e. But-1-yne.The reagents used are NaNH2, a…

Aromatic Compounds

Aromatic organic compound or aromatic system is an important class of hydrocarbons under the branch of organic chemistry. Aromatic compounds are also called arenas. The definition of aromatic organic compounds can be stated as a class of organic compounds with a planar cyclic ring of atoms bonded through alternated single and double bonds. Due to these alternating bonds, a peculiar feature termed as ‘resonance’, that is, delocalization of pi electrons or the electrons is shared within the atoms of the ring which are present in the aromatic compounds. The word ‘aromatic’ includes a Greek word ‘aroma’ which means smell, indicating that they were named as such due to the sweet odor they produce. Many well-known flavors such as vanilla, cinnamon, and few scents from flowers are extracted from aromatic compounds. Benzene with chemical formula C6H6 is a very common aromatic compound that contains six atoms of carbon held in the cyclic ring of alternate double bonds. It is also to be noted that not all aromatic compounds contain benzene ring. This can be explained by Huckel’s rule.