butan-1-ol butanal, CH3 CH2 CH2CHỎ. eq. NaOCI TEMPO 1 РСС NaOCI НОАС EtMgBr H;O+ H,CrO4 ether or PCC NaOCI НОАС H2CRO4 or PCC excess NaOCI ТЕМРО H2CrO4

Q: 1) n-BuMgBr/Et:O a) Butanenitrile 2) Н-О 1) DIBAH, toluene b) Isobutyl Acetate 2) H;O* 1)…

A:

Q: ÇH3 k. + methanol H3C, L. Ph-CI + H2O --- f. H2N-CH2-CH(OH)-CO2H [(R )-isomer] HNO2/HBr

A: Introduction: It is a way of depicting molecules in purely textual form. condensed formulae are the…

Q: 1. Give IUPAC names fro the following alkyl halides: (a) CH3CH2CH2CH2I CH3 CH3CHCH2CH2CI (b| (c) CH3…

A: Since you have posted a question with multiple subparts, we will solve the first three subparts for…

Q: 13) Complete the following reaction + O-C₂H5 2 eq. PhMgBr 1) Et₂0 2) H3O+

A: Esters react with Phenyl magnesium bromide in dry ether followed by hydrolysis give tertiary…

Q: 5. Draw the Zaitsev products. Br NaOCH3 NaOEt Br NaOH NaOCH Br 6. Draw the Hofmann products. Br…

A: 5.) According to Zaitsev rule, the beta hydrogen elimination takes place on that carbon which…

Q: 1) Na, CH3OH A. o-Xylene 2) NH3 1) R2NH, H", - H20 B. Cycloheptanone 2) EtHC-CHCOEt 3) НО +

A: Since you are posted with multiple sub-parts. As per the rule, i am answering first three sub-parts…

Q: CH3 CH3CH2. 1. ВНа ÇH3 0 1 NaBH, or LIAIHA 2. H,0 CH3 2. NaOH, H2O2 CH2CH2CHCH2ČCH3 a) b) CH2CI2…

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Q: f) CH3 Raney Ni /H2 g) CH2CN 1. LAH/ ether. - NH-C-CH3 h) 2. H20 ahot meing

A: In the presence of a reducing agent like NaBH3CN the iminium will be reduced to give a new amine.

Q: (1) (2) (3) Reagents a Br2 CH212 / Zn(Cu) / ether e i 1. O3 2. Zn / H30* b. CH31 H2 / Lindlar…

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Q: (d) Complete the following reaction: hv (i) Cp2TiMez +2 [RCH=CHR] AIMe:

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Q: el chloro - 2- propanone b) 4 Hy drexy- 4- mthyl- 2- pentanune c) - pentanene I, 3 - Cyclo…

A: Condensed structural formula is the shorthand way of writing chemical formulas. In a condensed…

Q: 4. Deduce the type of each reaction below: (a) CH2 CH3 CH3 CH,Ċ=CH2 + HBr CH2 CH3 CH3 CH2 CCH3 Br…

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Q: 1. Give IUPА names fro the following alkyl halides: (a) CH3CH2CH2CH2I (bl CH3 (c) CH3 CH3CHCH2CH2CI…

A: Since we answer up to 3 subparts, we will answer the first three. Please resubmit the question…

Q: complete.itbe.following Reaistontlall) ether. Hyot oues. periodimam 2 CH, myAf ether

A: This have multiple subparts questions, so I will solved first three subparts for you and rest of…

Q: OH 2 points 10. 11. HO CH2

A: We have to give the IUPAC name of the following compounds :

Q: 1. LIAIH,, ether major product 2 H,0°

A: We have given the organic reaction and we have to find the major product of the reaction.

Q: H;C-H2C + Ph;P=CH-CH3

A: Given

Q: Which of the following compounds is likely the least reactive in dilute aqueous NaOH? A. EtCOCl B.…

A: The question is based on the concept of organic reactions. we have to explain which of the compound…

Q: leianments Write All products indicate possible and major and minor where appl CH-CHs neat CHoll…

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Q: 7. (R)-3-methyl-1-pentene을 다음 4가지 시약으로 반응시켰을 때 생성되는 화합물의 구조를 그리고 광학 이성질체 여부를 설명하시 오. H CH3…

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Q: Cuando se añade H-Br a un alqueno terminal el producto sigue la regla de Markovnikov. O a. Cierto O…

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

Q: mCH3 व्कnशम्परिवककाट ९वmm-hio १Tmphithihe ) athic hydorophilic hx৭00१h०bic IC

A: There are 14 carbons in the long chain and this is an alkene . Its name is tetradecene. In this…

Q: e) 9-bromo 5-methyl 2-nonene -----H2, Ni 900°C---------- ? (name, str, stereochem) Cl2, CH2C12 f)…

A: Note: According to our guidelines we are supposed to answer only first three subpart . Kindly repost…

Q: This reagent produces alcohols from alkenes and adds primarily in a Markovnikov orientation     1)…

A: This reagent produces alcohols from alkenes and adds primarily in a Markovnikov orientation :

Q: H. Mg HC-C-I CH3 Et0

A: Magnesium metal reacts with an alkyl halide in the ether solvent to form Grignard reagent. The…

Q: i) CH2 = CH2 Reagent: Conditions: to CH2OHCH2OH CH3CHCH2 ii) CH;CH2CH,Br Reagent: Conditions: to…

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Q: H30* CH3CH2CH2C=CCH2CH,CH3 CH3CH2CH2CH2CCH2CH2CH3 H9SO4

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Q: f) g) h) i) j) Br of CH3 H3C CH3 Br 1. NaOEt 2. H₂, Pd/C Hg(OAc) 2 H₂O, THF -C=C-CH3 -MgBr (xs) Na…

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Q: PCk H,-Pd BaSO4 CH;NO, 1,0 CH;O OCOC- CH;0 CO,H СНО NAOH (Rosenmund reduction) OCH3 OCH3 OCH3 OCH3…

A: PCl5 is a chlorinating agent. In Rosenmund reduction acyl chloride is reduced to an aldehyde.…

Q: frocide all OEt olia A. Breleauivalento -> Ethanol/Na DEt Cons) 4. HCL Benzoyl peroxide

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Q: Draw the major product for each part. 1. BH3-THF 2. H,б, NaOH (a) KMNO4, NaOH, cold (b) 1. LIAIH, 2.…

A: 1. Hydroboration reaction reacts alkene followed by NaOH, peroxide gives alcohol to less substitited…

Q: Complete the following reactions: а. H Mg H,0 H,C-d CH3 Et,0 b. H3C KCN CI H3C с. CH,0 Na* H, C-…

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Q: se? ect one: a. 4-bromo-1-pentene b. 3-bromo-1-pentene c. 5-bromo-1-pentene d. 2-bromo-1-pentene…

A: In nucleophilic substitution reaction,  carbocation intermediate is formed.  3-bromopent-1-ene is…

Q: What is the reagent? OGMU Me-N OGMI OGMUL OMe OH ? Me-N OMe O

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Q: Complete these SN2 reactions, showing the configuration of each product.

A: SN2 reaction or bimolecular nucleophilic substitution has following features: Formation of a…

Q: E Noite the endenae ctruchure of Hhe pa lUoringi Wrüite the concenae' ņ 5,5- dinekye -8- heptene 2)…

A: We have to write the condensed structure of the following given compounds as follows in step 2:

Q: H NaNH CHICH Sa DH 1,0, who. gso H0 KMO HO, 10C Na kebne and akehyde O, M ethe. O- (excess) CHICH-Mo…

A: The alkyne shows various  type of Reaction With Various type of Reagents.

Q: H2NOC CONH2 CONH2 R N= H2NOC Co 'N N. H2NOC .CONH2 NH НО O. O=P- ОН R = 5'-deoxyadenosyl, CH3, OH,…

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Q: PLEASE DRAW OUT PRODUCT H2 Uz, 1 1. HONO 2. 2.CUBr Raney Ni NO2

A: 1,3,5,7-Cyclooctatetraene (COT) is an unsaturated derivative of cyclooctane, with the formula C8H8.…

Q: CH3 CH3 OH .CI ? SOcil2 a. N-chiorosuccinimide, light b. PCI3 c. nd. C2. light e. anhydrous HCI /…

A: We have to give the suitable Reagent

Q: Carboxylic Acid Resolve the reactions.

A: KMnO4 converst alkene to cis-diol K2CrO4 oxidizes R group with at least 1 benzylic CH to COOH Jones…

Q: Which halide is most reactive in SNl reactions? Select one: CI CI H3C CI CH3 CH2CI CI

A: The SN1 reaction is a nucleophilic substitution reaction. It is a two-step reaction where the first…

Q: I. Dom stoucfural fr mulas of Strucfural H alkanı e 2 me thy! 2,3- dimethyl a methy! 3 methyl cyclo…

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Q: NaoH cyclopentane deivatve ? Ø is phonyl cyclic kip unsaturated systew Naom

A: The details solution for this is provided below in attach image.

Q: Give the organic product + HÖ-CH;CH; CH;CH3 OH II OCH2CH3 H OCH2CH3 OH ČH2CH3 ČH2CH3 OH II IV H…

A: The reaction given is,

Q: H3C-C-0-Ĉ-CH3 A FeBr3 + Br2 B (Para Product only) AICI3

A: We have given the organic reaction and we have to find the major product of the reaction.

Q: 4020 of tHh ब ै tely volume of Rota noutralized の +KO牛fae

A: Mass of KHP = 1.020 g Molar mass(MM) of KHP = 204.23 g/mol Moles of KHP = mass/MM      =…

Q: Complete the reaction map by providing the answer from A-E. Write the IUPAC name of the products.…

A: Electron donating group increases electron density to ortho and para position. Thus electrophilic…

Q: 16) SN1 S-2-bromohexane C,H;OH +

A: In SN1 reaction two isomeric products are formed.  In first step formation of carbocation takes…

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.