9. NAHSO3 CH3 – C- CH3 19). 10. _(10a)_ NaOH → HC-O-Na + _(10b)__

Q: P. Putiday O2 CH3 P.Putida O2 6)

A: P. putida is a gram negative bacteria which helps to oxidise the ring by incorporating oxygen atom…

Q: Draw the substitution and elimination products.

A: “Hello. Since you have posted a question with multiple sub-parts, we will solve the first three…

Q: I Complete, these aguatien, identify and name the major produd. :) CH3 CH, CH, CH, CH = CH, + HI→ 2)…

A: Major product of reaction 1 ,2 ,3 - According to Markovnikov rule in addition reactions to…

Q: when necessary. a) b) Br2. H20 HCI d) H2 Ni MCPBA 1) ВН; THF 2) H2O2 NaOH f) H2SO4, HgSO4 H3O*

A:

Q: ဝ a) H3NCHCNHCH₂CO₂ CH3 -N=C=S 1) NaOH 2) anhydrous CF3COOH 3) aq HCI HN- H CH3 CI + Hဒ္ဒNCH၇CO2H

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Q: 9. NAHSO3 CH3 - C- CH3 19)_ 10. (10a) NaOH → HC-O-Na + _(10b)_

A: These are the oragnic reactions which include organic compounds that breaks or combines to give a…

Q: H PhH₂CH₂C PhH₂CH₂C H 14 .... CH3 4 CH3 mcpba mcpba ? ? HT/H₂O H™/H₂O ? ?

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

Q: Br,/CH3COOH ÓCH3 16 H,CH2COOCC COOCH2CH3 H2C excess NaOCH,CH; CH;CH,OH 17

A:

Q: 8. H2N-NH- 9. CH3 RČOOH 10. 1. NaBH4 2. H20

A: Given reactions: We have to find the products of the reactions.

Q: 2. H H c-N: H H 3. H2C `CH2 IU,

A:

Q: Complete the following reaction equations by supplying the formula of the missing reactant or…

A:

Q: 4. (4a) + NaHCOз - H2O + _(4b) 5. CH3COOH ± CH;CH2OCOCH3 + Hо -СОСН 6. _(6a)_ (6b)_→ + H2O

A:

Q: 9. NAHSO3 CH3 - C- CH3 10. _(10a NaOH HC-O-Na + _(10b)_ +

A:

Q: a. NH3 + H- i: *NH4 + :Ci b. Н,ӧ: + FeBrs Hö-FeBr3 0: +OH + H- ¢İ: HO, + :çi: HO, с. H H

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Q: 1) ? 2) ? 3) ? BRCH2CH2CCH3 HC=CCH2CH2CCH3

A: The conversion from reactant to product requires 3 step process including protection of the ketone…

Q: H3C CH,OH H,SO, CH3 H3C- H3C- H3C- H3C- OH H3C- OH H;C- OH OH 0-CH3 H3C-O -CH3 H3C-O -CH3 H3C-O A C

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Q: CI CI он OH HO А — Clz/H20 В -СНCI3/КОН С — 1. Оз/СH2CI2 2. Zn/HзО* D- HIO4/THF/H2O E - H3O*/THF…

A: A. Cl2/H2O: This causes conversion of alkene to trans halohydrin B. CHCl3/KOH: This generates…

Q: Nal Br acetone Br OD -MgCI CI t-Bu Меm 1 equiv. KOH ELOH C/

A: Alkylbromide is more reactive than alkenylbromide Grignard reagent reacts with alcohol to produce…

Q: CH3-CH2-O-H K,Cr,0, H,SO4 Heb abipe K,Cr,0, H,SO, -HO- CH;-CH,-S-H + NaOH CH3-CH-O-H + NaOH

A: K2cr2o7 in acidic medium is strong oxidisaing agent  It convert 1°alcohol into Aldehyde and 2°into…

Q: (е) H H H- C C- NH, H H Br Names:

A: The reaction taking place is given as,

Q: OM HBr+ 10.0 mL 1.0 M NaOH O M HBr + 10.0 mL 1.0 M CH3NH3*CH (pKb CH3NH2 1 O M HBr + 10.0 mL 1.0 M…

A: As we know,  Acidic solution has pH less than 7.  Basic solution has pH greater than 7 . While…

Q: IV. 1. 2. 3. H Fill-in the missing the reactant, reagent, or major product. 1. Hg(OAc)2, H₂O 2.…

A:

Q: So (J/molK) So Organic Substance AHC AG ΔΗρ AGº Substance (kJ/mol) (kJ/mol) (kJ/mol) (kJ/mol)…

A: I had filled all the values is table  Using the formula  ∆G= ∆H-T∆S

Q: MezNH (MeCO)20 Brz / AICI3 A ZnClz /100 * CH;CI2 1 кон 2.benzaldehyde MgBr E D 2. H20

A: Step 1 : Acetylation at 2 position of furan. Step 2: Bromination at 5th position of furan. Step 3 :…

Q: 9. OH CrO3, H2SO4 acetone H. YZA AZY AZY YZA

A: The question is based on the concept of organic reactions.   We have to identify the product formed…

Q: 4. (4а)— + NaHCOз - Н.О _(4b). 5. CH3COOH + CH;CH2OCOCH3 + H20 COCH3 6. (ба). (6b)__→ + H2O "OH

A:

Q: Complete the reaction below: OH OCH3 CH3I

A: The product of the above reaction is given below,

Q: CH20- NH2 1 NONO2, HCl 2. HB FH

A:

Q: OH OH (1) NaOH - (x) (2) H® Reactant x is : 7. (a) CH3CI (b) CH 2C12 (c) CHCI3 (d) CCl 4

A: Given reactant is phenol and product is salicylaldehyde. This is Reimer-Tiemann reaction.

Q: 2) Complete the reaction: CH3CH2C1 AIC13 NH CH3

A: Reactions involving organic compounds are called organic reactions.  Organic reactions are of…

Q: The answer choices give me chemical reactions like: C6H11FO3S + C5H11+ + H2O ---> C5H10 + C5H11+ +…

A: Given reaction is  We need to write overall reaction

Q: Show how to bring about  conversion

A: Given reaction:

Q: Br NaOH -> ace tone 11 CH3

A:

Q: benzoic acid, HC-H;O: K, = 6.6 x 10-5

A: As we know,  For acidic buffer,  pH range, pH  =pKa +-1 Now,  we know, pka of Benzoic acid  pKa =…

Q: Structure IV is an example of но но. он он он но- но- но- но- но- но- -H HO -H H- -он H- -OH H- OH…

A: Concept - Monosaccharides are the simplest carbohydrates since they cannot be hydrolyzed to smaller…

Q: (c) H₂N S HS. -N H

A: C. Given that, a transformation reaction is We have to give the mechanism for the above…

Q: NOME N CIATURE HO 이 Ha OCH CH CH 23

A: During the IUPAC naming of a chemical compound, we have to follow the given points --- i) At first,…

Q: 2NaOH CO Na HCI O-O CI + O-H H20, 0-5°C C

A: First step is formation of sodium phenoxide ion.

Q: 14СО, осcиr Occui

A:

Q: Draw a stepwise mechanism for each reaction.

A:

Q: ON OOH CN ÇHO -CH 3 OH CH3 CI

A:

Q: 1. sodamide, NaNH2 2. formaldehyde, HCHO 3. Нзо" -%1-hеptanol, CHз(СHг):СH2ОН Е. ? (name, str) -4.…

A:

Q: Complete the following reactions. OH e) KMn Oq Ho Hz C-0- CHz CH2 HI

A: The given reactions are represented as follows:

Q: NaOH H;C--o-CH3 H;C- Na но-сн, + H20

A: Addition of nucleophile  Loss of leaving group  Proton transfer

Q: Cl- 1. AICI3 CH2CI2 (solvent) 2. CH:NH, 0: 3. NABH4 MEOH (solvent) Cl Cl

A: These are the examples of intramolecular Friedel-Crafts acylation followed by reductive amination.

Q: Peacciones presentadas siguen el mecanismo SN1 o SN2. 1 H3C CH,01 CH,OH CH CH,COO-1 H3C Br CH,COOH…

A: SN2 preferred primary alkyl halide to give nucleophilic substitution reaction while tertiary alkyl…

Q: 8. C,H,O (aldehyde) 100- 80- 60- 40- 20 O 20 20 30 40 144 50 58 60 80 86 90 m/z 100

A: Molecular formula : C5H10O. (DBE = 5-(10/2)+1 = 6-5 = 1. Therefore compound name is n-pentanal.…

Q: OTBS PCC F) DCM, 25 °C 1) Hg(OAc)2. THF/H20 2) NABH4. Na OH TIPSOTI, pyridine H) DCM, 25 °C

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.