K (Most stable intermediate) CC, dil. H,SO, M N (Product) (Minor E1 product)

Q: (a) The rate-determining step for the reaction is (A →C, C → E, or E → G) (b) The fastest step in…

A: The reaction profile diagram is given as follows:

Q: Show the Reaction of a 1° ROH with HX—An SN2 Mechanism ?

A: SN2 Mechanism refers to a bimolecular nucleophilic substitution mechanism. Ex: ROH + HX -> RX +…

Q: In the box to the left of each reaction below, write the mechanism by which it occurs (could be SN1,…

A: As per rule only three subparts can be answered.

Q: How to find if a reaction is SN1,SN2,E1,E2 ?

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

Q: The products of the given reaction are, E2 CH;CH,Br H,C=CH2

A: In Nitrogen containing Lewis base its lone pair of electron is present in sp2 hybrid orbital ,which…

Q: What happens to the rate of an SN1 reaction under the following conditions? [RX] is halved, and…

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Q: Draw the major product and state wheter the reaction is SN2, E2, SN1, or E1

A: 1. Sodium tertiary butoxide is bulkier alkoxide ion , it acts as like base hence it abtsract beta…

Q: Draw a detailed mechanism showing the formation of the product, be sure to draw all intermediate and…

A: Radical Halogenation: In presence of light (hv) alkane with halogen reacts to form a halogenation…

Q: 1. For each of the following pairs of SN2 reactions, indicate which reaction occurs faster: a)…

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

Q: What nucleophile is needed to convert (CH3)2CHCH2CH2Br to attached product?

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Q: Rank the reactive intermediates by decreasing stabilization, most stable first. (ranking, e.g. like,…

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Q: How does each of the following changes affect the rate of an E2 reaction? (d, e, and f)

A: E2 reaction is a single step elimination reaction. As this is E2 , so it is bimolecular elimination…

Q: 1 .CO2CH CO2CH3 H20 | H2SO4

A: Diels-Alder reaction mechanism proceeds through the suprafacial (same-face involvement of the ?…

Q: or the two-step reaction sequence shown below. H,O2 BH3 THF HO Product-1

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Q: 1. For each of the following pairs of SN2 reactions, indicate which reaction occurs faster: CH;CH;Br…

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Q: Which mechanism is going to predominate under these conditions? A SN1 B SN2 LHOT HCI or C E1 D E2 O…

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Q: What happens to the rate of an SN1 reaction under the following conditions? [RX] is tripled, and…

A: Nucleophilic substitution reactions are those reactions in which nucleophile attacks the alkyl…

Q: 0° CN is a nucleophile . hence it strong undergo SN2 Kh. CN CNO SN2

A: Both the anions undergo substitution reaction because both are good nucleophiles and good…

Q: Rank the following molecules in order of increasing relative rate of SN1 reaction with methanol,…

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Q: in each structure circle the most likely site of EAS reaction 6. In each structure, circle the most…

A: EAS reaction means Electrophilic Aromatic Substitution reaction where the hydrogen atom of the…

Q: rate determining step for each an E1 and an E2 reaction including intermidiates /

A: The elimination reaction takes place when two atoms or a group of atoms leaves the reactant molecule…

Q: Br A Br B Br C D -Br

A: SN1 reaction The SN1 reaction is a nucleophilic substitution reaction where the rate-determining…

Q: Which one favors E2 reaction? A) isopropoxide ion B) tert-butoxide ion C) ethoxide ion D)…

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Q: cwhat is the inner sphere mechanism of this reaction:- 2+ [COCNH3)sd]

A: A chemical reaction that takes place between two coordination compounds in which transfer of…

Q: Draw a detailed mechanism showing the formation of the product, be sure to draw all intermediate and…

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Q: Rank these nucleophiles from best to worst Na- I -I Best (II)>(1)>(III) worst Best (1)>(III)>(II)…

A: A question based on introduction to organic chemistry that is to be accomplished.

Q: In the SN1 reaction, the 2nd step is the rate determining step. The SN1 reaction yields a total…

A: Given  In SN1 Reaction, the second step is the rate-determining step. The SN1 reaction yields a…

Q: What happens to the rate of an SN1 reaction under the following conditions? [Both [RX] and [:Nu−]…

A: The SN1 reactions stands for unimolecular substitution reactions. This type of reactions follows two…

Q: c) Propose a mechanism for this reaction. BF3 Но HO.

A: BF3 , boron triflouride is lewis acid. So lone pair of oxygen of -OH group attack on it and…

Q: Why does the final product has the opposite configuration compared to the reactant? Shouldn’t it…

A: Here, the given compound is secondary alcohol. When, methylsulfonyl chloride (or mesyl chloride)…

Q: is this an E1 or E2 mechanism for this reaction? What is the major product and mechanism for it?

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Q: SN1 is always a competing reaction of E1. True or False?

A: SN1 Reaction: A tertiary alkyl halide substitutes nucleophile by the removal of halogen as leaving…

Q: 10. (8pts each) Rank the reactivity toward the SN1 mechanism. Place answers in the box provided. CH₂…

A: Concept:  SN1 reaction: SN1 reactions are nucleophilic substitutions, involving a nucleophile…

Q: Rank the following substrates in order from slowest E1 reaction rate to fastest. Br Br Br Br A B

A: Given substrates,

Q: What type of mechanism is exhibited in the reaction? SN1, SN2, E2, E1?

A: In the given reaction, alkyl halide is primary and Nucleophile(KCN) is a strong nucleophile.

Q: Br or Br Br C or CI || CI or CI ||

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Q: Which reacts faster in an SN2 reaction? CH3CH2CH2Br or CH3CH2CH-BrCH3

A: SN2 is bimolecular nucleophilic substitution reaction. The reaction takes places in single step. The…

Q: Will each of the following reactions follow an El or E2 mechanism? CI HO Он

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Q: What happens to the rate of an SN2 reaction under the following conditions? [RX] is tripled, and…

A: The rate of an SN2 reaction under the given condition: [RX] is tripled, and [:Nu−] stays the same.

Q: Which substrate will go through E1 reaction fastest? Br Br A) B) ㅇ BY BV DJ ㅇ

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

Q: Draw the elimination product for the following reactions. Identify which will be the main product…

A: According to Zaitsev rule, in elimination reaction most substituted product will be more stable and…

Q: Which reaction proceed according to an E2 mechanism? toe. 3D II ethanol heat Br heat Br DMSO towe.…

A: E2 elimination generally occurs in the presence of heat, complete in one step and form alkene. As…

Q: If Zaitsev's rule does not apply and the base is bulky then how will the product look?

A: Bulky base like  potassium acetate will abstract beta proton from less hindered carbon to form less…

Q: From each pair, select the stronger nucleophile. Q.) CH3SH or CH3S-

A: The species which make a covalent bond by donating a pair of electrons is termed as nucleophile.…

Q: Br2/FeBr3 CO2CH3 SO/H2SO4 HO, CI AICI3 NO2 HNO,/H2SO4 CN

A: Reaction 1 : EAS ( Br+ is electrophile). Reaction 2 : EAS (SO3 is electrophile). Reaction 3 : Fridel…

Q: Which of the following pair of "Newman projection --> alkene product" schemes is most accurate for…

A: Answer is explained below.

Q: Based upon the following energy diagram, is this reaction an E1 or an E2 elimination? reaction…

A: E1 elimination reaction is proceeds via formation of intermediate, while E2 elimination reaction…

Q: What is a mechanistic step for this reaction? Click on a letter A through D to answer. fuming H2SO4…

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Q: Find the diene and dienophile for the following product (retrosynthesis): ? + ? B B

A: Retrosynthesis: When Reaction  is carried out from product to Reactant side Then reaction is called…