H 0: O-CH3 CH3OH₂+ protonati on CH3O OCH3 Draw Intermediate X CH3OH deprotonation - H₂O elimination > Н HO:0.0 Draw Intermediate H3C- 00: H :0. CH3OH nucleophi lic addition CH3

Q: What is the second step in the mechanism for the following reaction? CI HO. H CI H,O O Nucleophilic…

A: The second step in the given reaction has to be given.

Q: Sometimes carbocation rearrangements can change the size of a ring. Draw a stepwise, detailed…

A: The given reaction is an acid catalysed dehydration reaction of alcohols which are governed by E1…

Q: Draw a mechanism: OH OH heat LOH

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Q: What is the product of the following reaction sequence? O || SOC12 CH3OH CH3-C-0- A) CH3-C-0-CH3 B)…

A: This solution requires the knowledge of few chemical reaction.Carboxylic acid or carboxylate ion…

Q: HICIH Aree radical substitution mechanism componnd k It H H A HH H -C-C-C-C-C-C-c-H t Br, H CH3 4 H

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Q: Please answer these two questions   ProviGive IUPAC name of following compoundsde a detailed…

A: Enamine formation: We know that ketone reacts with amines in presence of acid to form enamine.We…

Q: Which of the following is expected to give a meso compound upon reduction with NaBH4 in methanol?…

A: NaBH4 can reduce aldehydes , ketones , acid chlorides and anhydrides.Meso compound is an achiral…

Q: H2SO4 / H,O / Heat HO ZI

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Q: Draw the mechanism of the transformation from 3 to 4. F EtO HO 3 OEt NaOH, MeOH HO OH

A: The objective of the question is to understand the mechanism of the transformation from compound 3…

Q: None

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Q: Choose the major product that is expected for the following reaction sequence: 1) NaNH, 2) Etl ?…

A: -> NaNH2 is base which can abstract most acidic hydrogen and form nucleophile.-> HgSO4/H2SO4…

Q: 1. Draw in the missing curved arrows in the following mechanism and identify the arrow pushing…

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Q: Which of the following is the major product of the reaction shown? OH ol C Ⓡ • O 11 111 IV V 11…

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

Q: Show the mechanism for each reaction. Determine if the reaction favors products or reactants. Use…

A: Whether equilibrium lies on the right side or left side depends upon the acidity of the reactant and…

Q: Which is the major product of the following Claisen condensation? C₂H ONa in C₂H5OH H₂C₂0 Sjoen…

A: The Claisen condensation is a carbon–carbon bond forming reaction that occurs between two esters or…

Q: Please re do over the work and check it it correct

A: Step 1: Basic mechanism of tautomerisation is:  Step 2: The correct mechanism is: Mechanism C

Q: Reagents with with ни он H no more than twoo carbons محمد H

A: This is an example of oxidation of primary alcohol to aldehyde

Q: Acetylation: tro S 요 :0: CH3CO₂H HH 11 OH H 12 HH CH3

A: Given reaction is an example of the substitution reaction of amine to form amide as a product.  i.e.…

Q: 1. Draw a mechanism to account for the following substitution reaction: CH3 CI CH3 H3C-N CH3 NaOH…

A: We know that hydroxide anion always attacks on the less substituted side. As less substituted side…

Q: Br

A: Note: According to our guidelines we are supposed to answer only one question. Kindly repost other…

Q: O-H + NAOH eloriools ons oibios alonert

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Q: Curved arrows are used to illustrate the flow of electrons. Follow the arrows and draw the missing…

A: Here we are required to find the intermediate and the product of the reaction.

Q: CH;CH, -Č-OH + KOH KOH What is a major product of the reaction above? OH CH,CH, C-OH CH;CH, C=0…

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Q: Draw the reactant of the following reaction shown

A: Robinson annulation Michael addition+intra molecular aldol condensation  carbanion  addition to…

Q: Incorrect, 2 attempts remaining H+ OH CH3CH2OH2+ :0 protonation Draw Intermediate CH3CH2OH…

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Q: Please re do over the work and check it it correct

A: Step 1: Step 2: Step 3: Step 4:

Q: Q4

A: Alkyl halide gives Substitution and elimination reaction

Q: H (03 H2SO4

A: Step-1: The alcohol(2-butanol) acts as base and abstract acidic proton from H2SO4. step-2: SN2…

Q: Draw the mechanism for the following reaction:

A: Please go through the reaction mechanism.

Q: CI H,0 А (substitution) e) -CH3 H,0 B + C (elimination) major minor

A: A substitution reaction is a class of chemical reactions in which an atom, ion, or group of atoms…

Q: Draw the product for the reaction in the space provided. H3C- CH3 CH H -CH3 + H₂O -> Select Draw…

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Q: O Provide the correct stuchre for intermediates A-M ) Mez Culi Socz NACN Br B PYndime D 2) H20 DLAH…

A: In organic chemistry, inter conversion of organic molecule takes place from one form to another form…

Q: Are the following reactions stere oselective? 1) (R)-2- bromo pentane reacts with CH3OH at room tem…

A: 1) not stereo selective (SN1) 2) stereo selective

Q: Choose the major product that is expected for the following reaction sequence: 1) NaNH, 2) Mel ?…

A: The given reaction is a multi step reaction in which alkyneialkyneis converted into carbonyl group…

Q: Draw the mechanism of the transformation from 3 to 4. F EtO HO 3 OEt NaOH, MeOH HO OH

A: The objective of the question is to understand the mechanism of the transformation from compound 3…

Q: H CH; CH;COOH A) H CH; HBr B) peroxides LCH; 1) BH3-THF C) 2) H.O NaOH

A: Solution- Answer is given below with structure and main product with the option wise;

Q: Reacti on Scheme:2ndrxn Ha sula (care) + Hzo HO n-butano I acetic acid n-buty acetate

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Q: Below is a mechanism that represents the following single reaction sequence: a certain ketone…

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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.