12. Under the right conditions radical bromination of A produces compound B as shown below (this is termed allylic bromination): hv Br2 -Br A Write a detailed mechanism for the propagation steps of the above radical bromination, showing how the products are formed and that the radical used in the first step is formed in the last step (use curved arrows to show electron flow).

Q: raw the starting alkyne that would lead to this ma under these conditions.

A: Hydroboration is the addition of boranes to the alkenes or alkynes to form the alkyl or alkenyl…

Q: 4. Show the mechanism for the formation of the Zaitsev product in the reaction below. Clearly show…

A: Typically, elimination processes take place in a way that removes a hydrogen from the carbon that…

Q: A student adds NBS to a solution of 1-methylcyclohexene and irradiates the mixture with a sunlamp…

A: NBS (N- Bromosuccinimide) acts as a source of Bromine free radical in bromination reactions.

Q: 2-methyl-3-phenyl butanoic acid OH O L CH3 CH3 PBr3 A Product for A Br₂, HBr B 2 equiv. Aniline…

A: PBr3 HBr Br2 Anilie NaOCH3

Q: 13.a. Give the mechanism(s) and product(s) for the reaction below. Show stereochemistry. CH3 H3C CH3…

A:

Q: Draw the starting alkyne that would lead to this major product under these conditions.

A: Hydroboration is the addition of boranes to the alkenes or alkynes to form the alkyl or alkenyl…

Q: 1. Use curved arrow formalism to propose a mechanism that can explain the formation of the following…

A:

Q: A student proposes the following two-step synthesis of an ether from an alcohol A and another…

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

Q: Identify reagents that can be used to achieve the following transformation: h The transformation…

A: In this question, we will synthesized the alkyne product from alkene starting material.  You can see…

Q: 11. A chemist performed the following reactions converting an alcohol into an alkyl bromide using…

A:

Q: Propose a mechanism for the following cycloaddition reaction. Classify the reaction using the [m +…

A:

Q: Can you explain the process of free radical bromination by using methylcyclohexane?

A: This reaction have done in three step.  Step1: Chain Initiation Formation of two free radical Step2:…

Q: 0-COCH3 1. H3C HCI OH OH 2. Aqueous acetone Br H20 HO. HBr a = Proton transfer d = Electrophilic…

A:

Q: This carbocation has the potential to rearrange to a more stable one. Part: 0 / 2 Part 1 of 2 Draw…

A: A carbocation is an important reaction intermediate in organic reactions. A less stable carbocation…

Q: 1. Rank the indicated hydrogen atoms in order of increasing ease of abstraction in a radical…

A: Radical Halogenation Reaction Radical halogenation is a type of organic reaction in which a halogen…

Q: 14. Based on the structural intermediates below, classify the role of the nitro group in the…

A: Nitro group is strong electronic widrawing group then the chloro group.

Q: 5. In the reaction below, only one of the alkenes react. Predict the product of the reaction and…

A: Approach to solving the question: Detailed explanation: Examples: Key references:

Q: 7. Propose a mechanism for the following Grignard reaction to show the structure of the product. 1.…

A: An ester  reacts first with a grignard reagent to form a ketone which reacts further to give an…

Q: 5. a) When the molecule below is treated with HCI, thế curved arrow formalism to draw a mechanism…

A: Carbocation has the tendency to undergo rearrangement from less stable carbocation to more stable…

Q: 6. What is the expected for the reaction shown below? Explain the major and minor products of the…

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

Q: Show how you would prepare the following molecules from the indicated starting material. More than…

A: In this reaction secondary alcohol group of cyclic D-glucose is converted into AzideN3 group. Only…

Q: to CH;CH,OH Br Major Minor Nucleophilic substitution mechanism:

A:

Q: HCI (conc) it

A: The electrophilic addition reaction of alkene proceeds in two steps. In the first step the proton…

Q: In this reaction, benzoyl peroxide ((BzO)2) is used as the radical initiator instead of light. When…

A: Benzoyl peroxide involves the homolytic cleavage by heat. Homolytic cleavage involves the…

Q: UESTION 4a structures. Provide the complete mechanism for product formation. Show all intermediates…

A: The objective of the question is to identify the product.

Q: 15. b) For each reaction below suggest structures for alkenes that give the indicated reaction…

A: a)

Q: The following reaction occurs at room temperature in acidic solution, first formingintermediate A,…

A: The question is based on organic reactions.    .  we need to identify the product formed and explain…

Q: Predict the monohalogenation products of these radical reactions, indicating major and minor…

A: There are many mechanisms in organic chemistry such as nucleophilic substitution, nucleophilic…

Q: 7. Give the mechanism and products for the multi-step reaction below. Clearly show stereochemistry…

A: EtONa: Good nucleophile, Favours SN2 attack Tosyl chloride: Makes OH a better leaving group NaCN:…

Q: 1. An alkyl chloride is treated with lithium diisopropyl amide, forming the following two products.…

A:

Q: 9. Predict the product of the reaction shown and provide a mechanism for its formation: HCI

A:

Q: Suggest a detailed step-by-step reaction mechanism for the reactions shown in a-b (use arrows to 8.…

A:

Q: 2. Give the mechanism and product for the recection below: ? NaOH A →

A: This is intramolecular aldol condensation reaction. In this reaction cyclic product are formed

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.