RO• make a polymer of 3 units or more CN f) ČN Draw the monomer

Q: HOH NaOH (1) 20N CH;CH2-Br PhCO,H () CI CHCI ČI CI OH (k) NaOH

A:

Q: (t) Cu) З Y- О ОН "OMe + En + En

A: Let us discuss step by step process for the formation of product.

Q: NH₂ HO HO

A: When 3 degree alcohol oxidized in presence of PCC / CH2Cl2 it converts into ketone

Q: ミッションX Cl b. / Hol プ れた。 ↓

A: Here we have to synthesize the following given compounds from the given starting materials by…

Q: 6. O H₂C 7. H₂C- 8. H3C H₂C OH -CH3 CH3 F + H₂O KMnO CH3 + NaOCH₂CH3

A: An alkyl fluoride undergoes the Hofmann elimination reaction irrespective of steric features in the…

Q: (а) но (b) -CH3 он (гасemic)

A: In this question, Reactants and Products are given and we used the Reagents to carried out this…

Q: Provide the major organic product of the following reaction. H3CH2C CH2CH3 HNO3, H2SO4

A: The given reaction is electrophilic aromatic substitution reaction. In this reaction nitration is…

Q: CI HC—CH, CH3 + HỌC–CH,CH, NH,

A: N-Alkyl-X-alkanamine

Q: Synthesize the products by drawing out reagents and intermediates along the way.

A: Since we only answer up to 3 sub-parts, we’ll answer the first 3. Please resubmit the question and…

Q: provide the reagen

A: 1. hydration alkyne to give enol first further it is tautomerised into ketone   2. NBS…

Q: 1) NaH 2) CH3CH2CH2B. РСС, THF NazCr2O7

A:

Q: d. KOEt EtOH NaOH, EtOH heat Jam Ph

A:

Q: b. H3C + H2O

A:

Q: KMNO, CH,CI AICI, heat FeCl, UINIO

A:

Q: CI HCI а. b. ethyne butanoic acid С. 1-propanol, H2S04

A:

Q: Show the synthesis for the following Reactions. M Ô olt Nit2 Br -NH₂

A: Please find the attachment

Q: СООН

A: Interpretation: The reagents and intermediate products for the following two-step reaction is to be…

Q: Kindly complete the following reactions and use IUPAC method to name the products.

A: To solve this problem we have to complete the given chemical reactions .

Q: Br NME2 HO

A: The crucial steps are in the given organic transformation are nucleophilic attack of amine followed…

Q: 4 H20, HSO4 9. Bra HO HCI 1. ВН-THF 2. НО, НО Нао МСРВА CH;OH H2SO4 7

A:

Q: Provide the major organic product of the following reaction. H3O', heat

A: In this question, we have to find out the correct answer of given problem by the help of the…

Q: Provide the reagents necessary to complete the following reactions. More than one step may be…

A: In this question, we have to synthesized the product from given reactant by using necessary…

Q: Na2Cr2O7 A H2SO4, H2O

A:

Q: `CI Ме

A: Here the starting material given is 2-chloropyridine

Q: OCH3 b) Ph Ph Ph Ph

A: The solution is s follows:

Q: Draw the two different major organic products of this reaction. Ignore inorganic byproducts. 0 TSOH,…

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

Q: CI Toluene 2-Chloro-N-(2,6-dimethylphenyl)acetamide dipropylamine Reflux 1 hour

A: Organic synthesis

Q: Br HO

A:

Q: 2. Reaction Fill-ins Predict and draw the product(s) OR starting material(s) for the following…

A: In part a there is ester formation .The reaction takes place between phenol and propanoic anhydride…

Q: 4 H20, HSO4 5 9. Bra HO HCI 1. ВН- THF 2. HO, HO, H20 МСРВА CH;OH HS04 7

A:

Q: QUESTION 5: NO2 SO3, H2SO4 Br2, FeBr3

A: ->HNO3/H2SO4 used for formation of nitrobenzene from Benzene. ->SO3/H2SO4 used for suphonation…

Q: 4. 5. OH + HCI strong acid catalyst

A: We have to predict the major products of the given two reactions. First reaction is the dehydration…

Q: Provide the reagents necessary to complete the following reactions.

A: Organic Reagents are an important part of the synthesis that helps in converting the reactants into…

Q: a. CH₂ b. H3C K C=C CH₂ H H + HF + H₂O

A: Markovnikov's rule says that the negative part of the addendum will attach to that carbon which has…

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.