Write a mechanism that accounts for the formation of ethyl isopropyl ether as one of the products in the following reaction. CI OEt HCI EtOH Write the mechanism for step one of this reaction. Show lone pairs and formal charges. Only the acidic hydrogen should be drawn out with a covalent bond. Write the mechanism for step two of this reaction (where the product of step one reacts with the solvent, ethanol). Show lone pairs and formal charges. Only the acidic hydrogen should be drawn out with a covalent bond. Write the mechanism for the last step of this reaction (formation of ethyl isopropyl ether). Show lone pairs and formal charges. Only the acidic hydrogen should be drawn out with a covalent bond. CI will act as the base in this reaction.

Q: ? 1 mol HBr H₂C 2 H₂ Pd 2 mol HCI ECH BH₂ ? H₂O₂, H₂O H₂C. -CH3

A: Given is series of organic reactions.Here, reactant given is alkyne.

Q: Complete these nucleophilic substitution reactions. In each reaction, show all electron pairs on…

A: These nucleophilic substitution reaction has to be completed. All electron pairs on both the…

Q: First Writedown which reaction it is? SN1, SN2, E1? Write a stepwise mechanism for the following…

A: Any molecule or ion which are electron rich species are called nucleophile for example -NH2,-OH and…

Q: Draw the structure of the major organic product you would expect from the reaction of 1-bromopropane…

A: Given,The reaction:1-bromopropane react with NaI.

Q: Starting from acetylene and alkyl halides not longer than 4 carbon atoms, show the synthesis of…

A:

Q: mark mechnism of catalysis

A: Solution: The given figures is the active sites of the metal-amino acids catalysis.

Q: Write a balanced equation to form sodium methoxide from methanol.  Choose a reactant that is strong…

A: Since methanol, CH3OH is a very weak acid, we need a very strong base like sodium amide, NaNH2.

Q: Predict the product formed in the nucleophilic aromatic substitution reaction between…

A:

Q: In essence, what I'm asking is, can we make a primary carbocation if it is next to a double bond…

A: A question based on reaction intermediates. Based on the stability of the carbocation, the given…

Q: The reaction of methylpropene with HBr, under radical conditions, gives twO intermediates. Propose a…

A: Given:-

Q: OH HPO4

A:

Q: + CH3OH methanol Suppose you were told that the above reaction was a substitution reaction but you…

A:

Q: Alkyl halides may be synthesized by reacting an alcohol with an acid (HX). Write the mechanism…

A:

Q: What reagents are needed to carry out this reaction? CH;CH,CH,CCH PCC in methylene chloride Sia2BH…

A: We will first determine the reagent for the conversion of above organic reaction then we will…

Q: Provide the product for the following reaction NH,NH2 KOH/ H2O/heat

A: The reagent NH2NH2 is known as hydrazine. It will give a reduction reaction with aldehydes and…

Q: c=CH H2O, H2SO4 H9SO4 `CH3 Alkynes do not react directly with aqueous acid as do alkenes, but will…

A:

Q: a similar fashion, draw intermediate 1 and intermediate 2 (final product) for the following reaction

A: Given is organic reaction. The given reaction is bromination reaction. This is an electrophilic…

Q: How many steps are in a reaction using an organometallic reagent? O 4 O 3 O 2 O 1

A: The reaction of an organometallic reagent with an aldehyde or ketone embodies the most fundamental…

Q: Ketones and aldehydes are hydrated under acidic or basic conditions. An example of the…

A: Final answer is given in explanation please see from there.Explanation:Approach to solving the…

Q: Complete each acid-base reaction and predict whether the position of equilibrium lies toward the…

A:

Q: Predict the products of this organic reaction: CH3 O CH3−O−CH—C—OH + NaOH Δ No reaction ?…

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

Q: diethyl heptanedioate i) Sodium ethoxide, ethanol ii) HCI, H₂O

A: The major organic products formed in the following reactions?

Q: NaOH NaOEt `OEt

A: 1. Hydroxide ion abstracts alpha proton of aldehyde to produce enolate. Enolate then attack another…

Q: CN H30°x, A X, COOH + NH4 X

A: In this given reaction hydrolysis of cynide or nitrile into carboxylic acid in presence of miniral…

Q: Inspect the structure of the following compounds and explain which one will elute first and which…

A: The objective of the question is to inspect the structure of the given compounds and explain which…

Q: -! Starting from ethane, outline a method of synthesis of meso 3,4 dibromohexane. SHOW ALL THE STEPS…

A: At first ethane is treated with one mole Cl2 under photolytic condition to get ethyl chloride. Two…

Q: Predict the product formed in the nucleophilic aromatic substitution reaction between…

A: Nucleophilic Aromatic Substitution Reaction : is a Substitution reaction in which the nucleophile…

Q: Determine the major product of the reaction shown in the box ن NaBH CH₂OH ON OH امه بلات C .

A:

Q: What is true about the reaction below? 1) Sia BH 2) H202/ OH O This is a Hydroboration-Oxidation…

A: The given reaction is Anti-Markonikov addition.

Q: Under milder temperatures than what is needed for dehydration, strong acids catalyze the…

A: `The formation of di-n-propyl ether from 1-propyl alcohol under strong acidic conditions is a…

Q: ÇOOH CH,OH CH,OH (1) LIAIH, (i) H̟O HNO, / H,SO, `NO,

A: The formation of alcohol from a carboxylic acid is a reduction reaction. It takes place in the…

Q: Which sequence of steps will give the highest yield of a carboxylic ester product? Mix 0.1 mole of…

A: Esterification is based on nucleophilic addition followed by substitution.

Q: 4-pyranone will readily undergo an acid-base reaction. Identify the reaction conditions that will…

A: The given reaction is shown below.We have to predict the product of the given reaction.

Q: The reaction below is an example of + O Acid-Base reaction O E2 reaction Hydrogenation reaction H₂…

A: The basic organic reactions types are addition, elimination, substitution, and rearrangement…

Q: Predict the product(s) for the following reaction, using as much acid and water as necessary: CH—NH…

A:

Q: Give a mechanism that accounts for the organic products of this reaction. Your mechanism must…

A: In SN2 reaction there is inversion in configuration. This is because nucleophile attacks from the…

Q: Reagents Available g. CO, HCI, CUCI/AICI3 h. CH3CH2CH2COCI, AICI3 a. CH2=CHCH,CI, AICI3 b. CH2Br2,…

A: The answer is as follows:

Q: N,N-diethyl-m-toluamide (DEET) is the active ingredient in many insect repellent preparations.…

A: Step 1: Step 2: Step 3: Step 4:

Q: following

A:

Q: H2NNH2 CH3 H* H3C `CH3 H3C IZ

A: We have find out mechanism for 3,5 dimethyl pyrazole

Q: Starting from acetylene and alkyl halides not longer than 4 carbon atoms, show the synthesis of…

A: NaNH2 acts as strong base and it can abstract proton efficiently from acetylene. BH2/H2O2/OH- is a…

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.