concd. H2S04 B + C heat 180°C 2) H2S NH2NH2 КОН KMNO4 F (CH3)2CHOH Br2/FeBr3 H heat NaOH LIAIH4 SOCI2 CH3O°NA* Br

Q: -H x Ⓡ

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Q: Synthesis Here are the targets. Starting compounds will be provided. 0. NHCH, starting Compound:…

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Q: From the figure above, what do you expect to observe in these reactions? Which mechanism? Which…

A: It is given that there are three alkyl bromides and two reagents A and B. Which reagent is best for…

Q: Ph. D-C-CH,CHO PHCH₂CHDCH₂CH=CHCH₂ CH₂CH=CHCHDCH₂CH₂P 0-0-04 0-0-040 Po OA OB hv Additional…

A: The Given Reaction is photolysis of aldehydesThe Aldehydes undergoes photolysis as follows:The…

Q: CI , AICI3

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Q: Consider the reaction scheme shown below. HCI [1] HO. (a) Provide a detailed mechanism for reaction…

A: This reaction will occur via 3 step. In first step protonation then Water molecule eliminate to…

Q: When the illustrated reagents are treated with a strong base the indicated reaction is observed to…

A: Witting reagent contains triphenyl as substituents and utilized in the generation of alkene. In the…

Q: Add curved arrow(s) to draw the final step of the mechanism. IO CH3 CH3 + Br: H3C Br: :ÖH CH3

A: When alkene react with per acid or m-CPBA to form given intermediate epoxide.  Cleavage of epoxide…

Q: 5. Draw the curved arrow notation and products for each elementary steps described by the sequence…

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Q: Draw the structures of compounds A–H in the following synthesis scheme.

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Q: c) Write the Ph Ph

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Q: 4. Propose a reasonable mechanism, using curved arrow notation, for the following reaction. Be sure…

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Q: For each of the following reactions, draw a complete, detailed mechanism and predict the major…

A: . When aluene react with Bromine in water medium we got addition     product . Nucleophite attack…

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Q: 7. Predict the product and draw a complete curved arrow mechanism for the following reaction. 1)…

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Q: Reaction: من Br2, HBr 1) NaOCH3 2) CH3Br 3) H₂SO4, H₂O, heat Sind. NaOH, H₂O 25°C ملح fla OH + en…

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: Provide a complete mechanism for the following reaction.

A: Information about the question

Q: Draw the product of the reaction where methoxide behaves as a nucleophile. Br H H H H + OCH3

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Q: 3. Provide a reasonable synthesis for the following transformations. You may use any reactions that…

A: The question is based on the concept of organic synthesis.We need to synthesize the product using…

Q: Give the complete detailed mechanism for the following reaction

A: In the given reaction the acid chloride reacts with methoxide ions to form an ester, by nucleophilic…

Q: Providwe detailed solution and give the explanation of the concept...

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Q: Compound below undergoes a Dieckmann condensation. Predict the product and draw the complete…

A: Dieckmann condensation: Intramolecular condensation reaction of diesters in the presence of a base…

Q: What is the product of the following sequence of reactions? NaOH NaNH2 H3O+ NH2 IV ||

A: An E2 elimination takes place where a chloroalkane is transformed into alkene. At first the Acidic…

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A: Pinacole-pinacolone rearrangement.

Q: write a complete stepwise mechanism to explain each of the following transformations be certain to…

A: This reaction proceeds in two steps. The first step is the removal of the leaving group to form a…

Q: earning Target 9 citeria for satisfactory score ementary mechanistic steps must be correctly…

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Q: 1) Me2NH, CH3CO2H 2) 3) H30*

A: We have to give the mechanism of the given reaction. Here the reaction goes through the enamine…

Q: (a) PHOOC-CH,-C-CH,-COOP. (1) KCN, A (2) H,0® (o) СООН Onl

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Q: Provide the curved arrow mechanism for the reaction of the compound shown below treated with…

A: Given compound contains -NHCH3 and -Cl- group on the ring. -NHCH3 group is electron donating group…

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A: This is the addition reaction of olefin,at first protonation occurs at the double bond and form a…

Q: 1. Propose a reasonable mechanism, using curved arrow notation, for the following transformation.…

A: We have to predict a mechanism for the reaction and include a transition state .

Q: 9) Predict the major organic product in following reactions: Al 6 PCC CLO 00/10 SOCI pili TIẾN NHẬP…

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Q: 3. Predict the intermediate and final products (A-D) for the following two reaction sequences. Then…

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Q: HBr ROOR CH,

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Q: 5. Predict the major product in the following reactions. MeO. CHO heat

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Q: Draw the complete, detailed mechanism (curved arrows) for the following reaction. Br 2. H₂O OK

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Q: Provide a detailed mechanism for the following reaction and give the major product. CI AICI 3

A: The Friedel-Crafts alkylation reaction is a classic example of an electrophilic aromatic…

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.