Q: 1. Give a synthetic route (hint: protecting group). OH
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Q: 5. Design a synthesis of the target molecule from the starting material shown. of ОН
A: Please find below the synthesis reaction.
Q: Classify following solvent as protic or aprotic CH3NO2
A: Protic solvents are those which contain protons bonded with high electronegative atoms like oxygen…
Q: Which or which of the statements given below is correct. I) Maleic anhydride is a carboxylic acid…
A: (I) Maleic anhydride is a carboxylic acid derivative which on reaction with water gives the…
Q: With an example describe mechanistically how an extraction is carried out acid-base.
A: Acid-base extraction is employed to separate acidic and basic compounds from a mixture.
Q: Design a synthesis for the following, using an intramolecular reaction:
A: Firstly, the reaction includes intramolecular Friedel crafts reaction resulting in the ring…
Q: NO2 NH2 Br NO2 НООС b. NO2
A:
Q: This is Wittig Rxn: Whatever mechanism you choose to draw is fine since you can leave the base as…
A: Wittig reaction is carried out between aldehyde or ketone and ylide to form the alkene .
Q: Design a synthesis that would lead to the formation of the desired product. Please provide arrow…
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Q: DMSO 0
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Q: Classify following solvent as protic or aprotic CH2Cl2
A: Protic solvents are solvents which contains protons bonded with high electronegative oxygen and…
Q: Perform a retrosynthetic analysis and suggest a synthesis of the target molecule (on the left) from…
A: The Retrosynthesis method is the method that determines the starting material by the fragmentation…
Q: Design a plausible synthesis for the following transformation. (The 3-carbon chain remains intact in…
A: We have to carry out given synthesis.
Q: Propose a reasonable mechanism using curved arrows for the following transformation. ОН heat ОН OH
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Q: Retrosynthesis for: OH Br product starting material
A: Retrosynthetic Analysis or Retrosynthesis is a planned approach for organic synthesis reactions. The…
Q: ore Br
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Q: At which position in the final product is there an ethyl attached?
A: Given that : We have to identify the position of the ethyl group in the final product :
Q: Q. Can anyone please show me the details steps involved in the retrosynthesis of the target…
A:
Q: Classify following solvent as protic or aprotic NH3
A: Aprotic Solvents are solvents that cannot display hydrogen-bonding. Protic Solvents are solvents…
Q: F;C. HCI ZI
A: IMPORTANT POINTS: In this type of question where precursor is asked ,here hypothetical hit and…
Q: Explain which position in indole will be susceptible to SEAr reactions
A: Indole has C3 position that is susceptible to SEAr, aromatic electrophilic substitution reaction.
Q: 5. Tropone (A) is much stronger base (conjugate acid more stabilized) than the open chain,…
A: Comparison of basic nature of A and B.
Q: Classify following solvent as protic or aprotic HCONH2
A: Protic solvent They have presence have O-H and N-H bonds. Protic solvent can participate in hydrogen…
Q: 2.) Design a reasonable synthesis for the following transformation. В.
A:
Q: Do a retrosynthetic analysis on the following compound, ending withavailable starting material.
A: Unconjugated dienes have the double bonds separated by two or more single bonds. They are usually…
Q: Please clearly draw the overall reaction taking place between methyl salicylate and sodium…
A:
Q: Propose a reasonable multi-step synthetic route that would accomplish the following Ph
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Q: Design a synthesis to accomplish the following in two or more steps. steps Bno.
A: 1. Reduction of Lactone with DIBAL-H.2. Condensation reaction of H2H(n-Pr) with the aldehyde.3.…
Q: The product (name) in the reaction with H20/ acid catalyst and H9SO4. Pls draw the whole reaction…
A:
Q: how would you deconstructing” a target molecule into its readily available, simple starting…
A: This synthesis involves Michael addition, aldol condensation, hydrolysis and decarboxylation
Q: Provide a reasonable mechanism, including all curvy arrows and intermediates, for the following…
A: A question based on mechanism of aromatic nucleophilic substitution, which is to be accomplished.
Q: Provide mechanism with curved arrows for Part B: Synthesis of benzil
A: PhC(=O)-CH(IH)-Ph on oxidation with HNO3 gives Ph-C(=O)-C(=O)-Ph which is called benzil. At first…
Q: Make a retrosynthetic analysis to design a synthesis plan. It should be ay least 2 steps synthesis
A:
Q: Do a retrosynthetic analysis on the following compound, ending with the given starting material:
A: Reterosynthesis is a hypothetical imagination to identify the starting materials to synthesize the…
Q: to
A: This synthesis involves Michael addition, Aldol condensation, dehydration, hydrolysis and…
Q: Propose a feasable synthesis of the target molecule (TM, Fig. 1) from the indicated starting…
A: This is the concept of reaction mechanism
Q: Use E1, sn1 or E2, sn2 Synthesis
A:
Q: Grignard reaction, 3-hexanol retrosynthesis, explain two methods.
A: Given target molecule is 3-hexanol. We can prepared it by using grignard reagent by using two…
Q: Explain the stepwise retrosynthetic analysis ?
A: Retrosynthetic analysis is used to convert target molecules into simple structures. These simple…
Q: 2) Show an acceptable mechanism for the following transformation using proper curved arrows. I1,0
A:
Q: Design a synthesis for the following reaction. If more than one step is needed, be sure to number…
A: Here we have to convert but-1-ene to butanoic acid in multistep reactions.
Q: 3. Please provide a complete step-wise synthesis of the target molecule showing all steps, reagents…
A: 3. Given reaction,
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: Thiatriazoles, when heated de-compose vigorously. Why is this?
A: On heating thiatriazoles decomposes to form nitogen gas and isothiocyanate. Because nitrogen is a…
Q: Chemistry Design a reasonable synthesis for the following transformation. E.
A:
Q: Why is the reaction of the type shown below usually done? a.To make an aldehyde or ketone less…
A: We've to predict the function of the reagent in the given reaction.
Q: 4. Provide a retrosynthesis only.
A: Retrosynthesis : at first three ethers are cleaved to give corresponding alcohols. Then functional…
Q: Explain Tautomerization with example?
A: Tautomerization
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