State Mechanism for Benzylic Bromination ?

Q: (d) 3-Methylpyridine N-oxide reacts with nitric acid and sulfuric acid to produce compound (19).…

A: In organic chemistry, compounds usually follow addition, substitution, or elimination reaction. The…

Q: Question is attached as a picture.   Thank you!

A: Tin metal and hydrochloric acid is a source of electrons and protons.

Q: 3. Among the products formed from PhC=CPh and Fe2(CO)9, is 2,3,4,5,- tetraphenylcyclopentadienone.…

A: Introduction: The formation of 2,3,4,5-tetraphenylcyclopentadienone takes place through the reaction…

Q: Give the major product (16) and the mechanism for the elimination reaction given below.

A: In this question, we will draw the major product with mechanism and explanation.  You can see the…

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Q: (a) Provide reagents for the following transformation. No mechanism is required. NH2 (b) Suggest…

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Q: Propose a mechanism for this reaction. A IC l3 HCI

A: The reaction given is known as Friedel crafts alkylation reaction. In the above reaction, the Lewis…

Q: (d) Propose a reaction mechanism to account for the following reaction. AICI3

A: In this question we have to tell the mechanism of the given reaction.

Q: Like other strong nucleophiles, triphenylphosphine attacks and opens epoxides. Theinitial product (a…

A: Triphenylphosphine attacks and opens trans-2,3-epoxybutane ring, the initial product (a betaine)…

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Q: Chemical equa tion when ethanal react with | in , Fehling test Schiff reagent EMn Oy 4 2.4-0NPH

A: the solution is as follows:

Q: Propose a synthesis of the compound shown below starting with benzene and any other acydic carbon…

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Q: Suggest a synthetic route for the following transformation. You should provide details on the…

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Q: Benzene magnesium bromide (Grignard reagent) reacts with acetaldehyde in diethyl ether to produce a…

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Q: H₂SO4 OH

A: mechanism of  the formation of the following compound, and an alternative product that could be…

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A: We have to suggest mechanism for the following reaction in step 2

Q: D. Provide reasonable mechanisms for the following reaction H NaOH, H₂O, A

A: Aldol condensation: The alpha hydrogen of carbonyl compounds is acidic in nature and it is removed…

Q: State the process of Addition of H2O to form an enol ?

A: Hydration of an alkyne will leads to form the enol intermediate and the ketone product in the…

Q: reaction of 2,5-hexanedione with P2O5 produces

A: Option A ( 2,5-Dimethylfuran ) is Correct

Q: an efficient and plausible synthesis for the following transformation. (use common Suggest reagents,…

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Q: Hów will you accomplish the following conversions ? Give plausible mechanism in each case,…

A: Synthesis of Furan derivative can be done by using alkyne and acetophenone as starting materials.…

Q: How might you convert cyclopentyl carboxylic acid to N-isopropyl cyclopentylcarboxylamide? Give two…

A: Answer -  Add N,N′-dicyclohexylcarbodiimide(DCC) along with Isopropyl amine, which will carry out…

Q: PROPOSE A MECHANISM FOR THE REACTION OF PYRIDINE WITH H2SO4 AND HNO3. ACCOUNT FOR THE…

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Q: b. Provide mechanisms and/or products for the following transformations. Pd°Ln, Cul, PhBr 1. HBpin,…

A: 2 b. 1-Hexyne reacts HBpin produces borate. It is used in the suzuki coupling. 1-Hexyne reacts with…

Q: What is the likely mechanism of nucleophilic substitution for attached alkyl halide?

A: Alkyl halides undergo nucleophilic substitution reactions. Nucleophilic substitution reactions are…

Q: POD 9: 02-10-21 Provide the Stepwise synthesis for the following transformation

A: In this transformation,  from a saturated lower analog,  saturated higher analog is formed.  Thus it…

Q: Br

A: Below attached file showing the details answer.  All the best.

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Q: propose a reaction mechanism for diazotization reaction

A: Propose a reaction mechanism for diazotization reaction --

Q: Suggest a synthesis of the following from benzene. You may use any additional reagents as necessary.…

A: Answer:- This question is answered by using the simple concept of chemical reaction of organic…

Q: Show the steps necessary to convert benzene into p-chlorobenzonitrilie, using a diazonium salt at…

A: It is an example of  electrophilic aromatic substitution

Q: Acid-catalyzed hydrolysis of HOCH2CH2C(CH3)2CN forms compound A (C6H10O2). A shows a strong peak in…

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Q: Explain mechanism - Base-Catalyzed Addition of H2O to a Carbonyl Group ?

A: Addition of H2O is referred to as Hydration. Compounds containing Carbonyl group such as ketones and…

Q: i H₂C H3C + CH3 LIAIHA [0] + [0] ?. ? Ethylbenzoate Give mechanism Acetic benzoic anhydride Give…

A: Please find the attachment

Q: Outine the synthetic sequence for preparing the following product from benzene. a) COOH b)

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Q: N(CH3)2 Cl. 1. 2. Н,О* N(Ph)2 1. СH31 2. HО*

A: The chemical reactions given are

Q: Q1/ Do as required: 1- The role of HSO, in Preparation of Nitrobenzene. Explain 2- The using of NaOH…

A: 1- The role of H₂SO4 in Preparation of Nitrobenzene. Explain 2- The using of NaOH with 2-naphthol in…

Q: Which of the following reaction is involves nucleophilic addition of carbonvl compounds? * Reaction…

A: In nucleohphilic addition , nucleophile add to the carbonyl group in the rate determining step .

Q: give the retrosynthetic analysis which has an aromatic starting compound that gives this product and…

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Q: The major product/s that form/s during the nitration of benzenesulfonic acid is? Choose the correct…

A: Nitration of sulphonic acid takes place as per following concepts.

Q: HBr HBr a) b) ? peroxides

A: Alkenes reacts with HBr without peroxide and undergoes addition reaction via carbocation formation…

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A: The answer is as follows:

Q: a. b. Br r_m

A: Detail mechanistic pathway is given below to carry out the following transformation

Q: Like other strong nucleophiles, triphenylphosphine attacks and opens epoxides. Theinitial product (a…

A: (a) Triphenylphosphine attacks and opens trans-2,3-epoxybutane ring, the initial product (a betaine)…

Q: x

A: Ozonolysis Treatment of an alkene with ozone followed by a suitable reducing agent to break down…

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.