1. An alkyl chloride is treated with lithium diisopropyl amide, forming the following two products. Determine the structure of the starting material and identify which of the two products is favored. What is the mechanism of this reaction?

Q: What is the major product generally formed when a tertiary alkyl bromide  (R3Br) reacts with sodium…

A: the solution are as follows:

Q: Each of these reaction produces ONE MAJOR PRODUCT. In each case, draw this product in the box…

A: Note : Since you have posted a question with multiple independent parts, we will solve first part…

Q: The following substances can be prepared by a nucleophilic addition reaction between an aldehyde or…

A: The given compound is a ketal. Ketals are formed when a ketone reacts with two equivalents of an…

Q: Predict the product formed in the nucleophilic aromatic substitution reaction between…

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Q: 1) Draw the complete electron-pushing arrow mechanism for the following reductions. Explain, using…

A: The given reactions are examples of birch reduction reactions.It is electron an transfer reaction.

Q: 6) You have decided to repeat the reaction from Question 5 using a slightly different alkene…

A: This question belong to reaction mechanism of organic compounds. Mechanism takes place via stability…

Q: 4. Show how you would perform the following syntheses. Provide the reagents and intermediates…

A: A) In the given synthesis the amide group is removed from the benzene ring.

Q: NaOH H20 Compound A Compound B

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Q: Propose a series of reactions that would convert the provided starting material into the given…

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

Q: Draw the major organic product of the following sequence of reactions. Show stereochemistry in the…

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Q: Rank the compounds according to their increasing reactivity toward electrophilic substitution. 1.…

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Q: 7. Provide the synthesis for the following product starting with the provide starting material. More…

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Q: Compounds X and Y are both C7H15Cl products formed in the radical chlorination of…

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Q: Predict the product formed in the nucleophilic aromatic substitution reaction between…

A: Nucleophilic Aromatic Substitution Reaction : is a Substitution reaction in which the nucleophile…

Q: Provide a detailed step-wise mechanism for the following reaction. Be sure to show all…

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Q: Show how the following starting materials are converted to the givenproduct by a series of two…

A: The pericyclic reactions are very useful in the synthesis of organic compounds. They occur in the…

Q: Give a mechanism that accounts for the organic products of this reaction. Your mechanism must…

A: In SN2 reaction there is inversion in configuration. This is because nucleophile attacks from the…

Q: Provide mechanistic pathway for each step and the products based on the reagents selected. Diels…

A: We have to give the product of the each step with the mechanism. The given steps are Step 1:…

Q: A chemist needs an ether to use as a solvent for a reaction and wants to synthesize it in one step…

A: Ether is a functional group which contains R-O-R group where R can be alkyl or aryl group.

Q: What is the source of the nucleophilic attack? How does the oxygen get protonated? What causes the…

A: Here nucleophilic attack , protonation and elimination occur in the given reaction.

Q: 4) Draw the complete electron-pushing arrow mechanism for the following reductions. Explain, using…

A: The given reactions are examples of birch reduction reactions.It is electron an transfer reaction.

Q: The Wolff–Kishner reaction uses hydrazine (H2NNH2) and hydroxide (–OH) to reduce a carbonyl to the…

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Q: Non-conjugated β,γ-unsaturated ketones, such as 3-cyclohexenone, as in acid-catalysed equilibrium…

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Q: ОН + …… ОН ОН

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

Q: H3C CH3 H3C CH3 Br NaH H.

A: Terminal alkynes on reaction with strong base, Sodium hydride (NaH) gives the corresponding…

Q: Tollowing two reactiOHS are performed on the same starting material; one producing "product 1" and…

A: Reaction (1) is the SN1 (unimolecular nucleophilic substitution) reaction in which tertiary alkyl…

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.