Perform the following retrosynthesis. OH NO2 NO, он Он

Q: The presence of bromine on a benzene ring - position(s). the ring but directs the electrophile to…

A: ->Electrophilic substitution reaction occur fast when there is maximum electron density in…

Q: CH3 CH3

A:

Q: Show the Reaction of a 1° ROH with HX—An SN2 Mechanism ?

A: SN2 Mechanism refers to a bimolecular nucleophilic substitution mechanism. Ex: ROH + HX -> RX +…

Q: OMe ? Me OMe ОН

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Q: Propose retrosynthesis and later synthesis LOCH3

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Q: Provide a synthetic pathway for the following transformation and draw intermediate structures. The…

A: Decarboxylation occur when carbanion is stabilized after leaving CO2....

Q: Show how to carry out the following transformation.

A: Alkyl brmides first give grignard reagent with Mg , from this reagent nucelophile is generated…

Q: Retrosynthesis for: OH Br product starting material

A: Retrosynthetic Analysis or Retrosynthesis is a planned approach for organic synthesis reactions. The…

Q: CH3 N. CH3 Но Ph

A: For retrosynthetic analysis one has to identify the compound, should have the knowledge of…

Q: Exl. OH Ph ) Ho A Ph KH,18-c-4, THF, (i) 2) NO2 Xylanes, hat NO2

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Q: NO2 CI

A:

Q: ROH .R Pyridine H3C

A: Here we have to write the mechanism of reaction in which ethanoyl chloride CH3COCl reacts with…

Q: OH (TM) (CH₂)4CH3 (SM) H

A: Here we have to synthesize the following given target compound from the given starting material by…

Q: 3. Show the series of step(s) to perform the following transformations. а.

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Q: Perform retrosynthetic analysis for the following target molecules and show how TO torward synthesis…

A: It is a technique used for solving complex molecules. The target molecule is transformed into…

Q: For each pair of aromatic compounds, determine which will undergo electrophilic aromatic…

A: Since your question has multiple sub-parts, we will solve first three sub-parts for you. If you want…

Q: Q. Can anyone please show me the details steps involved in the retrosynthesis of the target…

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Q: OMe cm Clz mCP BA MeO `OH

A: Given reaction is example of Baeyer-Villiger oxidation. The Baeyer–Villiger oxidation is an organic…

Q: Propose a reasonable mechanism. H*/ H2O

A: Given reaction,

Q: Qs1 Propose a correct synthetic route. Can be more than one. ÇOOH NO2

A: Since you have posted multiple questions in a single session, we are entitled to answer first…

Q: The reaction below is homogenic homolysis heterolysis heterogenic

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Q: CH3 H3C CH3

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Q: NEt, + CH;CH2CH,CH2Br + HNEt, H2N O,N он (a) (b) (c) (d) EIOH, H* NaOH, (b) (e) H;O* (a) (g) NET2…

A:

Q: 0. 1) СО2, Р, д 2) Н2О, H*

A: This is a klobe synthesis  in which major product is salicylic  acid

Q: Propose retrosynthesis and later synthesis OCH3 OCH3

A: Retrosynthesis and synthesis are given below for following structure -

Q: Show a detailed mechanism of the following reaction OH OH ATP H,0

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Q: 20) Provide the mechanism and draw the structure of the major product of the following reaction:…

A:

Q: propose the retrosynthesis of the following compound

A: The retrosynthesis of the given compound is-

Q: Propose this mechanism

A: Given reaction,

Q: Perform the following transformation and propose a mechanism Br ОН Br НО

A: When alpha-bromo ketone reacts with NaOH then to get carboxylic acid is formed. This is called…

Q: Meo ACOH MeO. NH2 NH

A: This is two step process. First step is the acid catalyzed imination of amine with aldehyde. second…

Q: An NH2 group_the ring toward electrophilic aromatic substitution by. a. activates, the inductive…

A: An NH2 group activates the ring toward electrophillic aromatic substitution by resonance. Option "c"…

Q: Show the mechanism for the nucleophilic aromatic substitution below. Br NH2 NaNH, ZON NaBr ZON

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Q: Show the retrosynthesis mechanism of this equation with curved arrows representing electron transfer…

A: Note : 1-Butene on hydroboration and oxidation produces the 1-butanol. Benzoic acid and 1-butanol…

Q: Complete the following transesterification reaction

A: Transesterification is the reaction of the exchange of organic groups between ester and alcohol to…

Q: 1) СО, Р, Д 2) H20, H*

A:

Q: Provide the mechanism for the following: CH3COOH + CH3 -OH O CH₂CH₂CH₂C CH3ÖCH₂CH₂CH3 + H₂O

A: We have to provide the mechanism for the given reaction.

Q: EWG EWG N. CI 2.

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Q: Provide the mechanism and the product for the following reaction. (HINT – pyridine is a Brønsted…

A: The given reaction undergoes from cyclic ester to cyclic amide with the help of given reagents.

Q: here would you cut during retrosynthesis for the following molecule 4 1l ansuuers

A: Given target molecule is beta hydroxy ketone , which is product of aldol condensation reaction.

Q: H H H. H,C H,C H,C H,C H H3C. H3C

A: Interpretation: We have to draw the curved arrows mechanism for the given reaction.

Q: How do I do the following multistep synthesis?

A: 1.Benzyl bromide is treated with grignard reagent to give alkylbenzene, further it is oxidised…

Q: acid esters Base Initiation Only meta para and meta lonic bonding Nucleophile Acid Chlorides…

A: solution~

Q: Show the retrosynthesis and the synthesis of the following compounds: OH Target material Starting…

A: Dear student, the given question is a multiple question, hence I solved first question according to…

Q: Propose a mechanism for cach of the following reactions ОН H2SO4 + H2O ОН

A: This reaction is the dehydration of alcohol by the formation of carbocation as intermediate. Hence…

Q: Propose retrosynthesis and later synthesis COOET EtOOC CH3

A: By retrosynthetic analysis, we actually try to move backwards on the synthetic line and try to reach…