The following reaction can be described by a THREE step mechani sm. A drawing of the energy diagram for this reaction is shown below. OH H,SO4 C B A Reaction coordinate (i) Write out the three steps in this mechanism. For each step, draw structures for the reactants and products and curved arrows to show bonds formed and bonds broken. (ii) Indicate which of the drawings in your mechanism corresponds to points A, B and C on the energy diagram. Draw the structure of the MAJOR product in the following reaction and an arrow pushing reaction mechanism to showhow the product is formed. H;O+ Potential energy

Q: What is the classification for this reaction? SO 3 + H 2O → H 2SO 4 double replacement…

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Q: The product distribution of the reaction below will consist of... QH HBr, A Br 4. Compound A…

A: Alcohol reacts with an alkyl halide to form an alkyl chloride. The reaction proceeds with an SN1…

Q: Complete energy diagram for the two-step conversion of A–B + C:−→ A:− + B–C

A: SOLUTION: Step 1: The overall reaction given is as shown below:   A-B + C: -→ A: - +B-C A possible…

Q: Rank  (1-4) from most reactive to least reactive (in decreasing reactivity in an elimination…

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Q: For the reactions below, will the product be B, C or both B and C? In the blank type B, C or BC (for…

A: For the blank 1, CN- will attack from axially and the mechanism followed will be SN2.

Q: 'N H CI H

A: The given reaction is as follows:

Q: Me Me X Me Me Me Br Me Me Me Nal, NaOCI EtOH, H₂O HNO3 Асон AICI3

A: Given are organic reactions. The reactions are electrophilic aromatic substitution reactions.

Q: 8. Assign an inner-sphere or an outer-sphere mechanism for the following reactions, and draw out the…

A: a) In the given reaction, since one of the reactants is substitution inert and the other one is…

Q: er. Br N- OEt N- OE

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Q: KOIBU OH H,SO, Br NaOEt

A: In the given reaction the alkyl halide present is a primary species and the reagent is a bulky base.…

Q: 3. Identify the products for the following reactions (no mechanism required) 1. Na MeOOC COOME 2. H*…

A: As per rules only three subparts can be answered of a question. The answers are as follows:

Q: Consider the product distribution of the following reaction. Use curved arrows to show the formation…

A: A carbocation is a positively charged carbon atom.It is considered to be an important intermediate…

Q: When the following reactions are carried out under the same conditions, the rate constant for the…

A: Since we know that in the E2 mechanism we need to break the C-H or C-D simultaneously along with the…

Q: 8-8 Identify the major product(s) of the following reactions. Include stereochemistry. (a) (b) (c)…

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

Q: 3. (a) In the following reaction scheme, identify the missing reagent or reagent combination in each…

A: Active methylene are those compound which have most acidic hydrogen.

Q: 10. What is the major organic product generated in the reaction below? Ho HO..... .. (A) OH (B) 1)…

A: Ozonolysis of the double bond produces the ozonide intermediate which is further decomposed by the…

Q: didention the following organic reactions as substitution elimination, or addition of from arrows to…

A: This question belong to reaction mechanism of organic compounds. Substitution Reaction: one…

Q: (5 points) Identify the electrophile and the nucleophile in each of the following reaction steps and…

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Q: HI There is no reaction under these conditions or the correct product is not listed. OH OH OH

A: this is addition reaction, HI is attached to given reactant where double bond get converted to…

Q: Draw the products for the following chemical reaction. Use the "Insert Image" button to add your…

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Q: None

A: The progress of a reaction can be represented by the reaction coordinate diagram. In a reaction…

Q: Refer to the following reaction: CH3 KOH a) Provide a detailed mechanism for reaction. Label each…

A: We have to provide the detailed mechanism of the given reaction.

Q: How many alkenes are formed by eliminating HBr from 3-bromo-3,4- dimethylhexane using NaOCH3,…

A: The objective of the question is to find the number of alkenes formed after eliminating HBr from…

Q: C) Please draw "A", "B", and "C" here:

A: Given are organic reactions.The given starting compound is acetylene.

Q: Choose the correct missing reagent/condition for the following reaction. To preview the image click…

A: Choose the missing reagent for the following reaction: Alkyne -> alkaneIn the given reaction,…

Q: CI CH3CI / AICI 3 H₂C CI

A: First of AlCl3 produces electrophile. After that electrophile will react with chlorobenzene and as…

Q: Does the equilibrium lie to the left or to the right in the following reaction: Н—С—ОН + CH,- O: ??…

A: Equilibrium lies in left or right in the reaction = ?

Q: Propose a reasonable mechanism for the reaction, drawing out Lewis structure, using arrows to show…

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Reactions of Ethers

Ethers (R-O-R’) are compounds formed by replacing hydrogen atoms of an alcohol (R-OH compound) or a phenol (C6H5OH) by an aryl/ acyl group (functional group after removing single hydrogen from an aromatic ring). In this section, reaction, preparation and behavior of ethers are discussed in the context of organic chemistry.

Epoxides

Epoxides are a special class of cyclic ethers which are an important functional group in organic chemistry and generate reactive centers due to their unusual high reactivity. Due to their high reactivity, epoxides are considered to be toxic and mutagenic.

Williamson Ether Synthesis

An organic reaction in which an organohalide and a deprotonated alcohol forms ether is known as Williamson ether synthesis. Alexander Williamson developed the Williamson ether synthesis in 1850. The formation of ether in this synthesis is an SN2 reaction.