Arrange the Alkyl chlorides in the order of reactivity in SN2 reaction according to the data you obtained and compare it with theoretical order of reactivity. Are they the same? If not comment on why there is discrepancy.

Q: The compound below is treated with N-bromosuccinimide (NBS) in the presence of light. Draw both…

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Q: Explain the difference between Zaitsev elimination and Hoffman elimination in E2 reactions. What…

A: When alkyl halides have two or more different β-carbons, more than one alkene product is formed. In…

Q: Identify the starting materials that can be used to produce the compounds shown using a Diels-Alder…

A: The question is based on the concept of diels-alder Reaction. It is the reaction between diene and…

Q: 22. Which of the following WILL NOT act as a diene reactant in a Diels-Alder reaction? A) OCH3

A: The Diene which will not participate in diels alder reaction is given below

Q: Friedel-Crafts alkylation of benzene with (2R)-2-chlorobutane and AICI, affords sec-butylbenzene. a.…

A: a) The Friedel-Crafts alkylation of benzene with (2R)-2-chlorobutane and AlCl3 gives secondary…

Q: Please explain why or why not the diene will or will not react with maleic anhydride.

A: The diene with the following are preferred- 4pi electron in conjugation, conjugated, less sterically…

Q: 1. Circle the aromatic molecules NOTE: bicyclic compounds with just one aromatic ring are still…

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Q: Alec wanted to prepare to diene B to use in a subsequent Diels-Alder reaction. He thought he could…

A: (a) Requirement from question: FT-IR data We will take FT- IR of the compound and will compare the…

Q: The diene shown below will NOT react in a Diels-Alder reaction. Why not? Select one: O A. The…

A: Diels alder reaction represent a type of cycloaddition reaction in which a conjugated diene react…

Q: Cannizzaro reaction has carried out using 3.1 mL benzaldehyde and strong base. What is the yield of…

A: The balanced equation is  2 C6H5CHO + KOH → C6H5CH2OH + C6H5COOK. here the reduction product is…

Q: Friedel-Crafts

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Q: 4. The following compound undergoes an intramolecular Diels-Alder reaction. Show the mechanism and…

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Q: Nucleophilic addition. Indicate the order of reactivity of: ethanal, 3-methyl-2-butanone,…

A: We have found out the reactivity of carbonyl compounds with nucleophilic addition.

Q: Why is the reaction more favorable at lower pH?

A: From the main question, we have the equation  3Co + 2NO3- + 8H+ →3Co2+ + 2NO + 4H2O We will discuss…

Q: Given the following reaction involving a diene and dienophile answer the following questions. A.…

A: To solve the problem, we need to address the following parts: Part A: Drawing the Two Possible…

Q: 2.) Give the product that would be obtained from each of the following Diels-Alder reactions (draw…

A: Diels - Alder reaction is a type of pericyclic reaction in which a diene cyclizes with a dienophile…

Q: Using the Grignard reaction, NBS, NaCN and any other reagents, synthesize Phenylacetone from…

A: We have to prepare Phenylacetone from Toluene using grignard , NBS , NaCN and some other required…

Q: Which of the following structures, A or B, has the faster rate of reaction in a Diels-Alder…

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Q: How many stereogenic centers are present in the cocaine analogue below? N. CO2CH3 OCOCGH5

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Q: Which of the following two compounds do you expect to be a better electrophile, and why?

A: The electrophiles are species, which are electron deficient and it can readily accept electrons. The…

Q: a. H CO₂CH3 CO₂CH3 H b. CO₂CH3 H H CO₂CH3

A: This question belong to Pericyclic Compounds. Diels-Alder reaction that is [4+2] Cyclo addition…

Q: (b) The activating and deactivating groups could affect the position(s) of the next incoming…

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Q: Consider the reaction of chloro, bromo, and iodocyclohexane with KOH to give the eliminatic product…

A: a) Iodide, which is the least basic of the four common halides (F, Cl, Br, and I), is the best…

Q: i-Pr O What product(s) would you expect to obtain from acid-catalyzed hydrolysis of the single…

A: Given that, an epoxide is We have to give the acid-catalyzed hydrolysis product of the above…

Q: What protecting group might you use on the problematic compouind above to allow for a Grignard…

A: Protecting a functional group refers to the process of chemically modifying a reactive chemical…

Q: 1-Explain why the reactivity is more for primary alkyl halide in SN2 and tertiary alkylhalide in SN1…

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

A: Diels-Alder reaction:During this reaction, three pi bonds will get broken; two sigma bonds and one…

Q: 19. a. Label the reactive features, highlight the most reactive one, then highlight what it needs.…

A: Concept is based on cycloaddition reactions:   As per our guidelines we have to answer a,b,c only.

Q: Do not handwriting solution.

A: see below for the answerExplanation:Resonance structures of the radical (ANSWER): This reaction is…

Q: What is the purpose of CH3OH being the solvent? Isn't CH3S- the only reagent needed in order to go…

A: Here methanol act as solvent.  In substitution reaction solvent have two function.  1. Provide the…

Q: Rank each of the following compounds in decreasing order of reactivity towards Friedel-Crafts…

A: Friedel Crafts alkylation is the replacement of an aromatic proton with an alkyl group. This happens…

Q: Explain the mechanism for Friedel–Crafts Alkylation Involving Carbocation Rearrangement ?

A: The Freidel crafts alkylation is generally depicted as:

Q: Which one of these provides the strongest nucleophile in an SN2 reaction? a) HC=N b) NaC=N c) NH3 d)…

A: The nucleophilicity of the above mentioned compounds depends on the extent of the dissociation of…

Q: The diene shown below will NOT react in a Diels-Alder reaction. Why not? Select one: O A. The…

A: The objective of the question is to choose the correct option for the molecule given ragarding…

Q: Draw the products of the following Diels-Alder reactions. Indicate stereochemistry where…

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Q: 3) What is a nucleophile? Provide some examples of nucleophiles that would work well in the SN2…

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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.