Chapter 22: Q35. (page 911)
Question:What reagents are needed to convert phenylacetonitrile () to each compound:
Short Answer
Answer
Chapter 22: Q35. (page 911)
Question:What reagents are needed to convert phenylacetonitrile () to each compound:
Answer
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Get started for freeDraw the product when each compound is treated with either (CH3)2CuLi , followed by H2O , HCCLi , followed by H2O .
a.
b.
c.
Draw the product formed when pentanal (CH3CH2CH2CH2CHO ) is treated with each reagent. With some reagents, no reaction occurs.
a. NaBH4 , CH3OH
b. {1} LiAlH4 ; {2} H2O
c. H2,Pd-C
d. PCC
e. Na2Cr2O7, H2SO4, H2O
f. Ag2O, NH4OH
g. {1}CH3MgBr ; {2} H2O
h. {1} C6H5Li ; {2} H2O
i. {1} (CH3)2CuLi ; {2} H2O
l. The product in (a) , then TBDMS-Cl , imidazole
Fill in the lettered products (A–D) in the synthesis of (R)-isoproterenol, a drug that increases heart rate and dilates lung passages.
Question: Poly(lactic acid) (PLA) has received much recent attention because the lactic acid monomer [ ] from which it is made can be obtained from carbohydrates rather than petroleum. This makes PLA a more “environmentally friendly” polyester. (A more in-depth discussion of green polymer synthesis is presented in Chapter 30.) Draw the structure of PLA.
Write the step(s) needed to convert CH3CH2Brto each reagent: (a)CH3CH2Li (b) CH3CH2MgBr(c) (CH3CH2)2CuLi
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