F3C1 `CF3 trifluoroacetic anhydride CH;CH,OH H3C + CF3CO,H HO, H3C“ `CF3 H3C OCH2CH3 Unsymmetrical anhydride 1 Ethyl ester 2

Q: You are given the structure of W. H2C-O-C-(CH2)10CH3 HC-O-C-(CH2)14CH3 Н.С-О-Р-ОН ОН i. Classify…

A: The solution is given below -

Q: Refer to the schematic diagram below, what is compound D? | Conc. H,SO, a-naphthol Conc. HS0, acetic…

A: The answer is as follows:

Q: 1. LIAIH4 C6H5OH C6H5NO2 2. NaNO2+HCI Ethanoicanhydride + NH3 → А, it is reduced to → B LIAIH4 A…

A: Applying concept of organic synthesis and reagent.

Q: OH Br SnBu3 1) TMSCI / Et3N 2) PhMgBr / THF 3) H₂O 4) TBAF 5) H30Ⓒ (Ph)₂CuLi 1) NaOEt 2) CH₂l₂/Zn-Cu…

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Q: 2. Name the following drugs and name their pharmacological groups. H3CO HC1 он H3CO CI H2C, LOCH3…

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Q: 7. Naphthalene (CioHe) 8. acetanilide (CSHs-NHCOCH;) 9. uracil H. "NH

A: Introduction: Molecular structure shows the arrangement of atoms in a space. The organic structures…

Q: 4) 2 hy droxy 2 butana 5) 6 ethy! -3 heptanone 6) R,3 dichloro . 4 hexynal

A: Please find your solution below : Structural formula is a formula that represents the arrangement of…

Q: + CH3MgBr a.

A: Grignard Reagent, CH3MgBr does not react with double bond of  alkene. However, it readily reacts…

Q: OH CH3 - CH2- CH- C=N

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Q: CH3 CH3 1. (CF3CO0")2Hg, H2O CH3-CH-CH CH2 CH3-CH-CH-CH3 2. NaBH4 OH (CF3CO0"),Hg, = mercuric…

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Q: Draw the structure of the major organic product(s) of the reaction. H3C 1. DIBAH, toluene 2. H,0*…

A: DIBAH is a reducing agent which reduces carboxylic acid and its derivatives into carbonyl compounds,…

Q: CH,CH, NH, H,C. Br Br NaBH, Br2 FeBr, agua

A:

Q: Oraw Figure 2 in the space below, the synthesis of melatonin, for each step label the functional…

A: Given that, the synthesis of melatonin from tryptophan. We have to level the functional groups for…

Q: OH + alcohol immediate precursors MgBr CH3CH,MgBr A B H. `MgBr H3C D E F

A: Given,

Q: a. Oxidation of 2-pentanol. (K2Cr2O7/H+) →…

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Q: MEPBA , CH3

A: Alkene gives epoxidation reaction with peracetic acid or meta-chloroperbenzoic acid. The reaction…

Q: (d) porphine, often used in supermolecular chemistry as well as catalysis; biologically, porphine is…

A: we need to find number of bonds formed by the ligand porphine with metal ion

Q: Which one of the following is most soluble in water? a. CH3CH2CH2CH2CH2OH b. CH3OH с. Не-Clz, Kip 3D…

A: Since you have posted multiple questions, we are entitled to answer the first only.

Q: (iv) CHЗСООН Ethanoylchloride NH3

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Q: 5. CH3CH2ONA + CH3CH2B 5) + NaBr, 6. _(6a)_+ 2CUSO4. + 4NAOH » CH3COOH + _(6b)__ + 2Na2SO4. + H2O

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Q: In which of these substances is significant hydrogen bondingpossible: methylene chloride (CH2Cl2),…

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Q: * prel modular exa... 1. CаНsО Aldehyde Ketone Alcohol 2. C4H8O2 Carboxylic Acid Ester 3. CоН6 Arene

A: To find: The condensed structural form of C4H8O: as aldehyde as ketone as alcohol The condensed…

Q: Carboxylic Acids Derivatives Name the structure - Proper formatting 다. X OH

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Q: СНЗОН ? NaOCH3 Isatoic Anhydride O:

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Q: Name Condensed otruchire Line diagram or structural formula Type of compound 1-methoxybutane…

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Q: The following are the pigments of spinach. Please rank them according to their polarity.…

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Q: 0.39 mol of solid glucose (C6H12O6) is dissolved in 100. mL of water, what is the (w/w%)-(3 SF)

A: The (w/w%) is to be calculated

Q: 11. C,H,O₂ (ester) 100 80- 60- 40 20- 10 20 29 30 40 50 5 60 70 80 90 102 100 m'z 110

A: Molecular formula C5H10O2 (DBE = 5- (10/2)+ 1 = 6-5 = 1. Compound is having carbonyl stretch.

Q: 1) NaOEt 2) 1,5-dibromopentane 3) NaOEt 4) H3O*, excess heat acetoacetic ester

A: The structure of acetoacetic ester is given as;

Q: Draw the products formed in attached reaction.

A: It is a cross coupling reaction in which an organoboron compound reacts with aryl or vinyl halide in…

Q: N,N-Dimethylbenzamide OEt HN II. + 2 HN +] 2 ΗΝ IV. NH2 + 2 CH3MGCI

A:

Q: Select to Draw mCPBA Select to Draw OH pTsCl pyridine H₂ Lindlar's catalyst 1. CH3CH2MgBr 2. H3O+…

A: Draw the missing products or reagents in the given multistep synthesis.

Q: OH он HO, Dexamethasone

A: The IUPAC name of the given compound is -

Q: Draw the following compounds: A) (2S,5R)-chloro-2-ethylhexanoic acid B)…

A: Structure for the compounds (A), (B) and (C) is given below,(A) (2S,5R)-5-chloro-2-ethylhexanoic…

Q: CH3 N2 ÇH3 CH3 `CH3 HO3S N,N-dimethylaniline methyl orange

A: The reaction given is,

Q: Complete the following reactions: Br2 FeBr3 F3C HNO3 H2SO4 (CH3)3CCI AICI NO2

A: Br2/FeBr3 is a brominating agent HNO3/H2SO4 is a nitrating agent RX/AlCl3 is an alkylating agent

Q: Safari File Edit View History Bookmarks Window Help -97% Thu 11:27 AM Q E cvg.cengagenow.com Cengage…

A: Organic chemistryEsters are caboxylic acid derrivatives.

Q: 2-methyl-1-pentene + H,O) Addition (Hydration) Heat, Conc. H,SO, II Condensation CH,CH,CH,C-OH +…

A: The addition reaction in which the two reagent added together to form an single product without…

Q: Provide the major product of the SO₂H Cl₂ AICI

A: Given reaction is halogenation reaction. Cl substitutes ring hydrogen.

Q: Draw the organic products formed in attached reaction.

A: A carbonyl-containing compound with alpha hydrogens can undergo substitution reactions with…

Q: What is the major organic prou 0₂N 0000 D + HNO3 NO₂ H₂SO4 OH B NO2 NO₂ 66 с D

A: Organic reactions are those in which organic reactant react to form organic products.

Q: Mg MgBr 7) Culi Br 8) light 2-bromo-2-methybutane (racemic mixture)

A: Welcome to bartleby !

Q: Br Bromobenzene CO₂ MgBr + + Mg ether ether MgBr Phenylmagnesium bromide H3O+ O Mg* Br+ 0=0 om OH…

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Q: H3C-CH CH2 + HCI + H2 + Br,

A: Addition of HCl on an alkene is done according to Markownikoff's rule. According to that H is added…

Q: Give the chemical names of the corresponding structures for compounds A, B and C.…

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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.