Your wanted to make the following molecule through iodine addition OH 12 OH ohn NOT isolated C11H14 Ol2 mystery molecule isolated C11H13Ol However, they did not isolate the anticipated product. Identify the structure of the unknown and provide a plausible mechanism for its formation

Q: NH2 H* -H,0

A: Ketone when react with primary amine forms imine as a product.

Q: What is the major product from this reaction? HBr (2 equiv) Br Br Br Compound A ● Compound B…

A: Since you have asked multiple questions, we will answer the first question for you as per our…

Q: 2. Mechanism: H-O- - NOZ -0. NO₂ H 0: HNO3 H2SO4 + NO2 но-н --- O: 7 -NO2 -H504 + :6= •N=O: -H₂0 ZO:…

A: Benzene is an electron-rich compound. It undergoes an electrophilic substitution reaction. One of…

Q: 0 2 33 give products of this reaction and outline the meachanisms M₂0 Br CI Na OH 350% NaOH 350°C Na…

A: This is simple question of nucleophilic aromatic substitution reaction where the nucleophile is…

Q: 22) Pyridoxal pyrophosphate (PLP) can catalyze both a,ß-elimination reactions and B,y-elimination…

A: Pyridoxal phosphate: Pyridoxal phosphate is a small organic molecule and co-enzyme that helps the…

Q: ÇH 1 HC CI H3C. CHCHONA аcetona 2.

A: The reaction mechanisms are

Q: (b) Give the product and mechanisms for the following reactions. N. CI CI i) CH3CH₂CH₂COPh,…

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Q: Br- C4H§S2 CeH12S2Br2 + Br A B

A: The detailed solution of your question given below-- Since, we know that the E1 and SN1 reaction…

Q: 18. Suggest a plausible mechanism with structures of the following reaction: Br, H,0 CH3 CH2B.…

A: In the reaction mechanism of the above reaction, first the alkene will attack on the Br2 molecule as…

Q: (0) OH /H,0 HC-C-CH2-CH3 CI (i) H3C он H,O*/A H;C. CH3 H3C CH3 100% - 2020 docx (93 KB Oct 22, 2020…

A: 1) nucleophile OH will add in place of Cl  2) first oH will gain H+ and then H2O will eliminate and…

Q: d) Suggest a plausible mechanism for the following reaction : Ph3P Ph3P Pt Ph PPh3 PPh3 Pt Ph

A: I have given the answer in the explanation section. Hope you will understand that

Q: The following reaction failed to deliver the desired product, instead giving a molecule with a…

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Q: @ b) Br OH Br OH ») x

A:

Q: Identify the leaving group for a potential elimination of the following compounds. Compare the…

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Q: Draw a plausible mechanism for the reaction shown below. Provide explanations for each step in the…

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Q: OMe С101002 Mol. Wt.: 162.19 mp: 34-38ºc KOH MeOH CgHgO2 Mol. Wt.: 148.16 mp: 135°C ОН

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Q: MeO. OMe O 16 BBr3 DCM, rt 90% RO. OR O 13 R = H ] DMAP, DCM 17 R = Ac Et3N ACCI

A: is a reagent used to demethylate ethers especially aryl methyl ethers. It can be used at room…

Q: Can you do it and explain it? Show the mechanism. I only need the last two questions

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Q: b) c) SO₂Ph TMS Pd(OAc)2 Et3N, 100 °C Pd(OAc)2 PPh3, r.t. TMS a + SO₂Ph + SO₂Ph

A:

Q: *Give mechanism* H₂C *Give mechanism* *Give mechanism* H₂C H₂C H₂C CH₂ CH₂ CH₂ CH₂ HBr HCI H* H₂O 1)…

A: We have to mention the product and the reaction mechanism.

Q: Propose a mechanism for the formation of (A)

A: The formation of A goes through a double nucleophilic attack after the 2 eq. of sodium hydride…

Q: Bi(0TH)3-41-0 R-OH + BiloTfb-4rb0. R-0M DMF /MeDH 0. R-OAU R-0THP + DCM

A: In organic synthesis, the THP group is used as the protecting group for alcohols.

Q: Provide the mechanism EENHS/ EENH₂> T H- -DH Et mccan HO=H Et 1 -NH H₂C ko

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Q: b. mCPBA привет нян H до OH MgBr Mg НО Ф Br PCC TSOH ОН MgBr OH я PBr3 PBr 3 ОН НО ОН Br TSOH PCC…

A: Given that, the reaction schemes are shown below We have to draw the mechanisms of the reactions.

Q: Praetice Give a mechanism that is the reverse of the following reaction: H20

A: The reverse reaction steps are

Q: HBr но он H (-H,0) Br Br 1 2 он 1) Ph 1) NABH4 2) H;0 Ph 2) HCI, H,0 Ph 4 3 он ÓH C1H2402

A:

Q: H,SO4 CH3 C C CH3 + H20 CH3 CH2 CH3

A:

Q: OH Br CO2H CO2H .CO2H Br2 Na* OAc easily enolized

A: enolate generation followed by substitution

Q: pentanone with n-butylamine with the molecule below with a catalytic amount of acid: 성 NH2 +

A: Carbonyl compounds shows nucleophilic addition reactions due to presence of C=O group.

Q: Me Me O Me Ph Me Ph 1. KH, 18-c-6, THF 2. PHCHO 3. NH₂Cl(aq soin) 1. LIN(i-Pr)2 (1.05 equiv) THF,…

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Q: Show the mechanism for the following reaction

A: Step 1:Aldehydes can be oxidized to carboxylic acids in the presence of Tollens' reagent. The silver…

Q: ethanol HSO, (cat) HO.

A: Carboxylic acid reacts with Ethanol in presence of dil.Sulphuric acid  gives an ester with removal…

Q: ОН + Но-СH2CH2 H30* CH3CH2CH2COH H3CH2CH2C H.

A: The reaction taking place is given as,

Q: Write a mechanism for the hydrolysis of the following iminium chloride in aqueous HCl. N CI +…

A: The mechanism for the following reaction can be given as- Step 1: Nucleophilic attack of the water…

Q: Give the mechanisms for the reactions NH2 NEt3 Et BLOH Ph Ph EtOH Et Me Me N 1) LiAlH4 (excess) 2)…

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Q: Туре: МС UESTION 6 Which of the following reactions form the products shown? Choose all correct…

A: Here we have to determine the correct product formed in the following given reaction. Addition of…

Q: Write the mechanism and predict the most likely product in the following reaction NaOH ICH2CH3…

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Q: H-OS03H H20

A: Alcohol undergoes dehydration in presence of suphuric acid (H2SO4)  Protonation Loss of water…

Q: Can you please check to see if my synthesis steps and mechanism are correct? I have to synthesize…

A: In the second step, Br- do not abstract the -OH proton, but it does nucleophilic substitution (SN2)…

Q: A student proposes the following mechanism for a nucleophilic substitution reaction: Br: ? Notice…

A: The bimolecular nucleophilic substitution reaction is a concerted reaction that occurs in a single…

Q: Na SOH SO-H NANO2 2-паphthol MW 144.17 HCI NH2 NO II NaOH p-sulfanilic acid MW 173.19 a diazonium…

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Q: (CH3),COCH3 HI (CH3),CI CH3I H20 но e OH i) MgBr i) BrMg" ii) HO, HO, ii) H,0

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.