a. Explain why 1-bromo-2,2-dimethylpropane has difficulty undergoing both SN2 and SN1 reactions. b. Can it undergo E2 and E1 reactions?

Q: Explain the reaction and reactivity of halides tested towards silver ion in Sy1 reaction: o Arrange…

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Q: Explain why 1-bromo-2,2-dimethylpropane has difficulty undergoing both SN2 and SN1 reactions.

A: 1-bromo-2,2-dimethylpropane has difficulty undergoing both SN2 and SN1 reactions have to be…

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: Why we need step 3 before step 4? a. Because the nitro group increases the electrophilicity at the…

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Q: (E) An aprotic solvent is best for Sn1 reactions as they tend to help stabilize carbocation…

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Q: H2C Br

A: E1 elimination is a two step process in the first step leaving group leaves and forms a carbocation…

Q: Q4 Which statement below about Sn1 reactions is incorrect? (A) SN1 reactions are stepwise and have…

A: A chemical reaction mechanism represents the way to form and break the chemical bonds between…

Q: Rank the following dienophiles (from least reactive to most reactive) in terms of reactivity in a…

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Q: Compound 2 Me0z OʻK+ Compovnd3 Compound 4 compound 1

A: Robinson Annulation is Michael addition followed by intramolecular Aldol condensation.

Q: 4. Are there any RX compounds from part A that are not expected to undergo an Sn1 or SN2 reaction?…

A: Note: Chloro benzene, bromo benzene cannot participate in sn1 or sn2 due to unstable carbocation and…

Q: Alkyl halides 1-chlorobutane 2-chlorobutane Allyl chloride 2-chloro-2-methylpropane…

A: Allyl chloride    The electronegativity order of hybridized carbons is sp>sp2>sp3.  So in an…

Q: Which undergoes faster SN1 substitution reactions with hydrogen halides, 2° or 3° alcohols? Explain…

A: Since, you have asked to solved multiple questions, so I will solved first question for you.  You…

Q: Q4 Which statement below about Sn1 reactions is incorrect? (A) SN1 reactions are stepwise and have…

A: Given statements, (A) SN1 reactions are stepwise and have intermediates. (B) The slow step in a SN1…

Q: Which reacts faster in an E2 elimination, cis-or-trans1-bromo-3-tert-butylcyclohexane

A: Biomolecular elimination (E2) reaction:E2 reaction involves a one-step mechanism in which…

Q: How does changing the solvent from CH3OH to DMSO affect the rate of an E2 reaction?

A: The reaction in which one molecule is eliminated from reactant compound, such reaction is called…

Q: Which solvent conditions favor SN1 reactions over SN2? polar protic apolar protic polar aprotic O…

A: Sn1 reaction is unimolecular nucleophilic substitution reaction.  Sn2 is bimolecular nucleophilic…

Q: Rank the following compounds in order of increasing SN2 reaction rate with a good nucleophile.…

A: We have to rank the given compounds in order of increasing SN2 reaction rate with a good…

Q: Provide the reagents (in correct order) necessary to complete the following transforma CH3-CH₂-OH…

A: Given-> CH3CH2OH ---------->.CH3CN

Q: Explain why methyl vinyl ether (CH2 = CHOCH3) is not a reactive dienophile in the Diels–Alder…

A: Diels-alder reaction is a cycloaddition reaction in which two molecules combine to form a new ring.…

Q: What can cause an exception to Zaitsev's rule during E2 dehydrohalogenations? OA steric hindrance O…

A: To identify: What can cause an exception to Zaitsev's rule during E2 dehydrohalogenations.

Q: Rank the primary, secondary, tertiary, and aryl halides in terms of reactivity with the nucleophile.…

A: Nucleophilic substitution biomolecular reaction (SN2): The bimolecular nucleophilic substitution…

Q: Predict reagents needed to complete this SN1 solvolysis reaction. Br

A: Detail mechanistic pathway for SN1 reaction is shown below

Q: On a single graph, draw the reaction coordinate diagram for the addition of one equivalent of HBr to…

A: Given reactions, (1) Addition of HBr to 2-methyl-1,3-pentadiene: (2) Addition of HBr to…

Q: III. Which alkyl halide in each of the following pairs will react faster in an SN2 reaction with OH?…

A: The nucleophilic substitution reaction involves the removal of the leaving group with its bonding…

Q: 2. Write the synthetic procedure for the target compound with your own idea. (At least more than 5…

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Q: (i) Provide the product for the reaction below. (ii) How would you know if the reaction was an SN1…

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Q: 2. For the following Alkylhalide indicate which position will react under SN1 reaction conditions…

A: The nucleophilic substitution reaction involves the replacement of one group by other group and it…

Q: (i) Provide the product for the reaction below. (ii) How would you know if the reaction was an SN1…

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Q: 2. A limitation of the Friedel-Crafts alkylation reaction is that the presence of…

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Q: 1. Based on the theoretical result, what is the order of reactivity of primary, secondary, and…

A: Since you have asked multiple questions, we will answer the first one for you. To get the remaining…

Q: Which isomer reacts more rapidly in an E2 reaction: cis-1-bromo-4-tert-butylcyclohexane or trans-1-…

A: E2 elimination reaction : It is a type of elimination reaction that is mostly observed in the case…

Q: β-elimination reactions.

A: IN E2 REACTION THE H WHICH IS SITUATED IN BETA POSITION ARE ABSTRACT BY BASE AND ALKENE IS FORMED…

Q: SN1 reactions undergo carbocation rearrangments, but E1 reactions do not because the carbocation…

A: The given statement has to be given as true or false,

Q: CH3(CH2 )sBr NaOH CH3(CH2)5OH + Br + A) The rate would increase because SN2 reactions favor a polar…

A: Nucleophilic substitution biomolecular reaction (SN2): The bimolecular nucleophilic substitution…

Q: Iodoethane does not react via Sn2 reaction with NaI in Acetone. It is a good leaving group and on…

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Q: does methyl bromide favour SN1 or SN2 reactions or can be either depending on conditions ?

A: SN1 stands for Substitution Nucleophilic Uznimolecular. SN2 stands for Substitution Nucleophilic…

Q: The mechanism by which the haloform reaction works. Explain.

A: We have to give the mechanism of haloform reaction.

Q: There is an overall 29-fold difference in reactivity of 1-chlorohexane, 2-chlorohexane, and…

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Q: Which will react faster in SN2 displacement, 1-bromopentane or 2-bromopentane, and why?

A: The SN2 reaction is a substitution nucleophilic bimolecular reaction. In this reaction, bond…

Q: The formation of a carbocation is the rate-determining step for an SN2 reaction.  A.   True B.…

A: Given statement: The formation of a carbocation is the rate-determining step for an SN2 reaction. We…

Q: How does solvent affect rate of reaction if its increase or decrease in sn1 or sn2

A: In SN1 reactions, there carbocation intermediate so solvents of higher polarity  stabilizes these…

Q: Rank the following in order from slowest to fastest rate of reaction in a Diels–Alder reaction with…

A: Introduction: Diels-Alder reaction is a cycloaddition reaction of diene and dienophile to form a…

Q: hy is bromination more selective than chlorination?

A: bromination more selective than chlorination because

Q: B. What type of elimination reaction is this: E1 or E2? Explain. C. Explain how the leveling effect…

A: Explanation of mechanism : Dehydration of alcohol in presence of acid involves three steps.  1.…

Q: How does changing the solvent from DMSO to CH3OH affect the rate of an E1 reaction?

A: E1 reaction stands for unimolecular elimination reaction. As the name suggests these reactions…

Q: Which halides are unreactive in a Friedel–Crafts alkylation reaction?

A: The Friedel–Crafts reactions are a set of reactions developed  to attach substituents to an aromatic…

Q: Rank A, B, and C in order of increasing SN1 reactivity.

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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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Q: Arrange the substrates in order of increasing Sn2 reactivity with NaCN: (A) Bromoethane, (B)…

A: To solve this problem we have to know about the reaction order of SN2 reaction for alkyl halides .…

Q: 8. Explain why (1S,3R)-3-tert-butylcyclohexyl bromide undergoes E2 elimination with potassium…

A: E2 elimination is elimination reaction where the rate of the reaction depends on both the reactant…

Q: 4. Are there any RX compounds from part A that are not expected to undergo an SN1 or Sn2 reaction?…

A: Note: primary alkyl halides prefers sn2 reaction. secondary alkyl halides prefers sn1 or sn2 depends…

Q: Explain the reaction and reactivity of halides tested towards silver ion in Sy1 reaction: o Arrange…

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Q: In not more than three (3) sentences, explain why terminal alkynes are acidic.

A: Since you have asked multiple question, we will solve the first question for you as per our…

Q: Choose the best reagent for carrying out the following transformation: 1. LIAIH4, THF 2. H3O+ O 1.…

A: In these example ester is convert into aldehyde .

Q: How does changing the halide from (CH3)3CBr to CH3CH2CH2Br affect the rate of an E1 reaction?

A: E1 reaction proceeds with a two step mechanism where the first step is the formation of carbocation…

Q: After E2 elimination, will the following molecule contain deuterium? Why or why not?

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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.