Synthesize 3,5-dibromotoluene from benzene and any suitable inorganic and organic reagents. Assume you CANNOT separate ortho and para products and both isomers have to be carried through in the entire synthesis.

Q: :0: :0:- CH3 - CH2-C- CH3 OH CH3-CH=C-CH3

A: Ans

Q: CN DIBAL-H, -78 °C

A: DIBAL-H is a mild reducing reagent. DIBAL-H react with nitrile formation of imine followed by…

Q: Starting from the starting compounds, the synthesis given below Synthesize using inorganic reagents

A: The oxidation reaction adds oxygen to the organic compound. The aldehyde hydrogen can be made…

Q: Devise a synthesis of (3R,4S)-3,4-dichlorohexane from acetylene and anyneeded organic compounds or…

A: The structure of (3R, 4S)-3,4-dichlorohexane is shown below:

Q: ce CH3-C=CH 2 Hce CH3-C-CH3 ce

A: In the first step the terminal carbon atom of the alkyne will get protonated by one HCl molecule.…

Q: H-H ? ? ? H и Осозн

A: The question is based on the concept of organic synthesis.  we need to synthesize the product using…

Q: Provide The major organic products for each reaction

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Q: NH2

A: Naphthalene, on reaction with concentrated H2SO4 at 1600C gives 2-naphthalene sulfonic acid. On…

Q: From benzene, organic compounds with 6 carbons of less and any other inorganic compund you want.…

A: Given that : We have to synthesize the following naphthalene derivative from benzene :

Q: Propouse a retro-synthesis and a synthesis for the following compound.

A: Given: a compound To find: a retro-synthesis and a synthesis for the compound.

Q: provide synthesis for this reaction including all reagents and mechanisms with steps ↑

A: This can be done like this

Q: Provide the major organic products for the following reactions. KMN04 hot, conc. CI он NaOH NO2 heat…

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Q: CI 2HCI CH3-CECH CH3-C-CH3 CI

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Q: 3-methyl-1-pentene - (1) HI (2) t-BUOK, I-BUOH 1. H₂, Ni 2. EtOH, heat Product in Steo 1: Product in…

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Q: Devise a synthesis of (3R,4S)-3,4-dichlorohexane from acetylene and any needed organic compounds or…

A: The synthesis of (3R,4S)-3,4-dichlorohexane from acetylene is given below.

Q: H2O, H2SO4 HgSO4 CH3-CEC-CH3 + H2 Lindlar CH3OH A H2SO4

A: Please find your solution below : Alkynes on reaction with H2SO4 and HgSO4 give ketone by the…

Q: O usmg any othen Startng with acehe acid and necessang reagents, synthesize The following compornds…

A: 2 We have to synthesize the following given compounds by using any other necessary reagents starting…

Q: Starting from benzene, synthesize the following compounds. Write the complete reagent/s and…

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Q: OH CH3 OH CH3 CH3 CH3 OH CH3 OCH3

A: Organic reaction mechanisms.

Q: Provide the major organic products for the following reactions. H+ MEOH AICI3 NH2 acetic acid NaOCH,…

A: Ester undergoes nucleophilic substitution reaction in presence of H+/CH3OH.  Note: As per the…

Q: Give the two major organic products for the following reaction

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Q: Substitutions on aromatic rings are generally carried out by electrophilic substitution, but for the…

A: A question based on aromatic compounds that is to be accomplished.

Q: Provide the major organic products for the following reactions.

A: We have given the organic reaction we have to provide product of the reactions.

Q: OH O,N NH2

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Q: ? つ Ho

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Q: Carbon NMR Spectrum A has peaks at & 71, 40, 19, and 12. Spectrum B has peaks at 8 72, 38, 31, 29,…

A: The solution is as follows:

Q: Please devise synthesis of the product compounds below from their respective starting material.

A: Oxirane reacts with tertiary butyl amine to form an alcohol substituted product. On oxidation, with…

Q: Provide a stepwise synthesis to carry out the following conversion. CHÍNH,

A: In this organic reaction several multiple steps are involved.The following steps are involved.

Q: ОН Br ОН

A: For synthesis, first we have to block acid and alcohol group as ester and ether respectively .…

Q: f. o OH OH single enantiomer

A: step 1 : Reaction name ; Hydroboration Oxidation              Reagent ; IpcBH2…

Q: provide a synthesis with the starting being Benzene

A: Solution-  synthesis of the following compound with the starting being Benzene is drawn below;

Q: Complete the following syntheses by filling in the missing structures or reagents!

A: To complete the given synthesis by filling in the missing structures and reagents.

Q: Synthesize Chloramphenicol from Toluene or Benzaldehyde. Draw and explain step by step please.(p.s:…

A: Chloramphenicol is an antibiotic used to cure many  bacterial infections such as cholera, typhoid…

Q: Byphenyl synthesis From benzene, organic compounds with 2carbons or less, and any other inorganic…

A: The functional groups are the key constituent of a molecule and they offer a characteristic chemical…

Q: How is the mechanism for oxymercuration/demercuration reactions of alkenes understood?  How are the…

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Q: Starting with benzene and using any other necessary reagents of your choice, create a synthesis (or…

A: When benzene is treated with Chloro propane in presence of aluminium chloride, then Friedel crafts…

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.