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Q: 3) Withg rea etion a reachion n Sequences

A: Since we only answer one question, we’ll answer the first question. Please resubmit the question and…

Q: Most electrophilic CI OH EN NH₂

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Q: 3 Do a full conformational analysis for the highlighted bond. (note: CH₂ > Ce) the Br H ייוון Br ร…

A: To understand and visualize easily we will draw the molecule in Newman projection. Then keep any one…

Q: (don't use hend raiting)

A: The objective of the question is to identify which of the given species, CH3 or CH2, can be…

Q: Draw the skeletal (line-bond) structure of CH3CH2CH2CH2CH2COCI.

A: When drawing the skeletal structure of an organic compound, we should represent the carbon atoms at…

Q: Which of the following compounds are aromatic? Me. Fir -Me Me A C Select one: Oa. A and D only None…

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Q: Name the compllex CrCl2 (en)2. The oxidation number of chromium is +2. Enter the name.

A: Naming of coordination complex

Q: Which compound is a diastereomer of the structure shown? ОН ОН ОН II III IV There are no…

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Q: In which way can the following structure be rewritten? H-C- -C-C-H H. CH) CH, CH,-CH-CH; b.…

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Q: Identify from the following compounds which one is aromatic. OIV O III OV 01 O II || IV

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Q: Name the forrouing compounds a,

A: The IUPAC name of the compound can be written on the basis of the main carbon chain, functional…

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Q: In each set of reschace structures below, rank contribution that each resorice e structure makes to…

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Q: Select the most contributing resonance structure from each pair. A B C 1 N=CIO: НО. H R O CH3 O CH3…

A: When the bonding in a molecule cannot be expressed by a single Lewis structure, the resonance theory…

Q: Cit3 OH H2504 ProvidE the Stepwise mech anysm. use Curved arrows and show all formal charges on 9l…

A: Given: Reaction To find: To write the mechanism of this reaction. Solution: The reaction given is…

Q: a mixtuce he, Ds ,ace given the general fumula Fez Oy They yreted elemental an wten beentell to…

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Q: Draw EI - MS for CH3CH2CH2CH 2BR Explaining your resonance for the peaks show clearly.

A: The objective of this question is to show the mass spectrum of CH3CH2CH2CH2Br which show to electron…

Q: "en OH -NH₂ (9 Br он ) ૮૧ 12 NH₂

A: “Since you have posted multiple subparts questions, we will provide the solution  only to the first…

Q: (е) H H H- C C- NH, H H Br Names:

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Q: NaCN HCI KMnO4 E DIBAL 00 H+ I OH LIAIH4, H G CHỊCHINH2 Phcoo H 0 H3O+ H₂O

A: Friedel-Crafts Alkylation Replacement of an aromatic proton with an alkyl group through an…

Q: where did the other Br go

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Q: c) d) CN CH3 CN OCH3 CN CN CI CN beinud bns astsibsmmsini abubni anottosen gniwollat O

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Q: Synthesis of Aldehydes and Ketones

A: The mechanism of given reaction are provided below  in attach image.

Q: HSO E) CH,OH NaOEt F) CH,OH H,SO G) CH,SH NANH2 H) EIOH

A: All are epoxide ring opening reactions , mechanism is given below

Q: ) Draw t Name the first s alKanes (carbens 1-5) 2) Draw + Name the alkenes with 2 throngh six…

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Q: please represent the product with OH dashed and wedged la lines Tiloi-pr]y, t-BuOOH (+)-DET

A: This is Sharpless epoxidation reaction. This is enantioselective chemical reaction..In this…

Q: 1) LIN[CH(CH,kk (LDA) h) (H;CC THF/ 50'C Br N° Boć 2) Br

A: This reaction is an asymmetric reaction. In the first step, LDA abstracts a proton from the alpha…

Q: Identify from the following compounds which one is aromatic. 68{82 || ||| IV HeH N H IV N

A: The compound is known to be aromatic if it fulfills the following criteria-PlanarCyclic and…

Q: Which of these compounds is the Choose... most reactive with water?

A: Acid chlorides are more reactive than anhydrides which are more reactive than Easter ,which are more…

Q: Determining HB or not

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Q: A. Give the IUPAC name for each of the following: 2. H H H 1. H H H Н— с— с с — С С —н - Н— с- с — С…

A: The given compound contains a six-carbon atom chain, hence the root name of the compound is hexane.…

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.