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Q: What products are formed by hydrolysis of each imine or enamine?
A: The products are formed by hydrolysis of each imine or enamine has to be determined.
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Q: R1 NH N-R N=C=N, R `R1 A H2N. D .N. E ZI O=
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Q: What is the major product of the reaction of biphenyl with HNO2/H2SO4?
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A: On reduction of Carboxylic acid, aldehyde is formed.
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A: Intermediate that formed when C6H5CH2CN is treated with the DIBAL-H is;
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Q: i. 8-valerolactone j. 2-chloroethanoyl chloride k. formaldehyde 1. a-oxo valeraldehyde…
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Q: Draw the structure of the product formed when 2-methylbutanal is treated with cold aqueous base.…
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Q: Treatment of ethyl acetoacetate with NaOEt (2 equiv) and BrCH2CH2Br forms compound X. This reaction…
A: The structure of "X" in the formation of illudin-S by acetoacetic ester synthesis is shown below.
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Q: 18. When ester reads w excess LAH + water adiol is formed which diolio corredt mjor prod? O x9 LAH 0…
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Q: OH - NH, Br2/KOH →product; 1. (a-hydroxy amide) Product of this Hoffmann bromamide reaction is : OH…
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Q: Please draw out the 2 reaction schemes: Ethyl diacetoacetate + hydrazine = pyrazole Ethyl…
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Q: Draw the product formed when phenylacetic acid (C6H5CH2COOH) istreated with each reagent. With some…
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Q: Draw the product formed when phenylacetic acid (C6H5CH2COOH) istreated with following reagent. With…
A: Given reaction, Phenylacetic acid (C6H5CH2COOH) with NH3 (1 equiv)
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- Draw the product(s) formed when A is treated with each reagent.a. NaBH4, CH3OH b. LiAlH4, then H2O c. Ag2O, NH4OH d. CrO3, H2SO4, H2O e. PCCDraw the product formed when phenylacetic acid (C6H5CH2COOH) istreated with following reagent. With some reagents, no reaction occurs. SOCl2Nicotine can be made when the attached ammonium salt is treated withNa2CO3. Draw a stepwise mechanism for this reaction.
- Draw the product formed when pentanal (CH3CH2CH2CH2CHO) is treatedwith following reagent. With some reagents, no reaction occurs. Na2Cr2O7, H2SO4, H2OFill in the missing reagents a-h in the following scheme:Draw the product formed when phenylacetic acid (C6H5CH2COOH) istreated with following reagent. With some reagents, no reaction occurs. NH3 (1 equiv)
- Draw the structure corresponding to each name.a. 5-methylheptanoyl chloride b. isopropyl propanoatec. acetic formic anhydride d. N-isobutyl-N-methylbutanamide e. sec-butyl 2-methylhexanoate f. N-ethylhexanamideDraw the product formed when phenylacetonitrile (C6H5CH2CN) is treated with each reagent. I need help with D,E, and F.a. Is (R)-lactic acid dextrorotatory or levorotatory? b. Is (R)-sodium lactate dextrorotatory or levorotatory?
- Draw a stepwise mechanism for the conversion of lactone C to carboxylic acid D. C is a key intermediate in the synthesis of prostaglandins (Section 19.6) by Nobel Laureate E. J. Corey and co-workers at Harvard University.Draw a stepwise mechanism for the conversion of lactone C to carboxylic acid D. C is a key intermediate in the synthesis of prostaglandins by Nobel Laureate E. J. Corey and coworkers at Harvard University.3-Fucosyllactose is another HMO found in breast milk. (a) Locate any acetal and hemiacetal. (b) What products are formed when 3-fucosyllactose is hydrolyzed in aqueous acid?