Br2 -? CCI4

Q: Please provide detailed mechanism for this reaction.What is the role of Amberlyst I-120 plus resin?

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Q: Provide specific examples/reaction scheme/mechanism for each of the following: a) Hoffman…

A: Hoffman elimination: When a quaternary ammonium hydroxide is strongly heated it decomposes to yield…

Q: Enol form in the mechanism of * halogenation is present.step Fast Slow Both

A: Answer :- Enol form in the meachnism of halogenation is present fast step.

Q: Predict the major product of each of the following reactions and provide the complete, detailed…

A: (a) Alkane reaction with Br2 in presence of light is a free radical addition reaction.

Q: Draw the complete, detailed mechanism for the addition of hexan-3-ol to dihydropyran and predict the…

A: The given reaction is,

Q: d. Consider the following secondary halides. Changing the leaving group from fluoride to bromide…

A: Halides are good leaving groups. The tendency of the leaving group increases as the size of the…

Q: Draw the complete, detailed mechanism for the reaction shown here and draw the major organic…

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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…

Q: H2C (SYN) (a) Draw the alcohol that would be required to form the alkyl chloride shown here using…

A: The reaction between alcohol and phosphorous chloride (PCl3) results in chloroalkanes.

Q: Predict the product of the reaction between acetic anhydride and each of the following compounds. If…

A: As here question has multiple subparts, so solve first three subparts. If student want complete…

Q: Provide/ Draw the major product/s of the following reactions

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Q: Provide a multi-step synthesis of the target structure on the right from the starting structure on…

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Q: For each reaction, draw the complete, detailed mechanism and the major organic product. (a) (b)…

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Q: (e) When treated with base, the compound shown below cyclizes. Show the structure and relative…

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Q: The phenyl group, C,H, is known to be an ortho/para-directing group. (a) With that in mind, predict…

A: Para product is majored.

Q: Treatment of but-2-yne with NCS affords an interesting molecule with two methoxy groups and

A: N-chloro succinimide is abbrivated as NCS .  In presence of polar solvent Chloronium ion is…

Q: Please explain and draw the step by step mechanism of oxidation of alkynes with kmno4 and…

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Q: Br NBS, HV.

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Q: 9.42 Did the overall reaction shown here occur by an SN2, Sn1, E2, or E1 mechanism? How do you know?…

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Q: Draw the complete, detailed mechanism for the reaction shown here and predict the major products,…

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Q: Consider the following reaction scheme (note that the reagent shown above the arrow is DBN"). Draw…

A: DBN is a sterically hindered bicyclic non-nucleophilic nitrogen base.

Q: (SYN) Each of the following compounds can be produced from an alkyne, via electrophilic addition.…

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Q: An enamine, R2C=C-NR2, behaves as a nucleophile in much the same way that an enolate anion does.…

A: Enolate ions have two or more reactive sites so they are called, ambident reactive species. The…

Q: When phenyl-5-bromopentanone is treated with triphenylphosphine, followed by base, a compound is…

A: The structure of triphenyl phosphine is

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

A: “Since you have asked multiple question, we will solve the first question for you. If you want any…

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: Propose a complete mechanism for the following reaction. Be sure to use correct curved arrow…

A: The reaction is Friedel Crafts alkylation reaction. The reaction proceeds via the formation of a…

Q: Br, and light CC14 solvent

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Q: Provide a reasonable mechanism that provides the major product for the reaction scheme provided…

A: The reaction given is,

Q: Draw the complete mechanism and the major organic product for each of the following reactions.

A: The complete mechanism for a given reactions has to be given.

Q: different reactions with specific conditions given (i.e., reagent and solvent). -Please include…

A: Given; The starting material is propene. , CH3- CH2=CH2 Let's try to make an ether from propene. The…

Q: Draw a reasonable, detailed mechanism that shows this racemization at the a (alpha) carbon. Note:…

A: When the mixture of the stereoisomers (R or S) present in equal proportions, it provides a racemic…

Q: Give the complete, detailed mechanism for the following reaction. Be sure to include an explanation…

A: Given reaction,

Q: HO H2SO4 H2O, heat

A: This reaction proceed through E1 mechanism And the product of this reaction is

Q: please explain what happens in this reaction mechanism. be as DETAILED as possible. acetylene +…

A: Br2 is a covalent compound, there is no charge separation. But during the reaction there is a…

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

A: In the first reaction, since we have a nucleophile CN- and an electrophilic carbon in the reactant…

Q: Predict the major organic product of this reaction and draw the complete mechanism to form it: H2SO4…

A: See product in red box.

Q: Predict all organic product(s) that would be formed in significant yields from the reaction shown…

A: In this reaction due CH3- group and OH- group, different substituted compounds are formed. In all…

Q: Draw the complete mechanism and predict the products of the following Cl2 Fe or FeCl3

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Q: Here is a reaction leading to the formation of a racemic mixture of alcohols as products majors:…

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Q: Complete the mechanism for this acid-catalyzed transesterification by drawing out allthe individual…

A: Esterification occurs between acid and alcohol but trans esterification occur between ester and…

Q: Did the following overall reaction occur by an SN2, Sn1, E2, or E1 mechanism? How do you know? Draw…

A: In nucleophilic substitution reaction, nucleophile substitute leaving group but in elimination…

Q: Provide the complete mechanism using Curved Arrow Formalism for the reaction of benzoic anhydride…

A: Amine is a nitrogen containing functional group. It can act as a base or nucleophile. Carbonyl…

Q: Draw the complete, detailed mechanism for each of the following reactions, including the major…

A: All the reactions given above are Markovnikov addition reaction

Q: a) Draw a complete, detailed mechanism for the following reaction and label the rate- determining…

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Q: 1) NaOH H 2) H*, heat

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Q: Same reaction as previous question. Which statement(s) is(are) true concerning the rate-limiting…

A: We have to predict the correct statement regarding rate limiting step.

Q: Predict the major organic product of this reaction and draw the complete mechanism to form it:…

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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.