The synthetic sequences shown below are unlikely to occur as written. Tell what is wrong with each, and predict the true product. Br OCCCH3)3 (CH3)3COK H3C- CH2CH3 H3C- CH2CH3 (CH3)3COH OH NAOH OH CI CH SOCI2 CHs Pyridine (c).
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- Show the electron-flow mechanism of the synthetic schemes (R-Salsolinol) of the picture below. This involves predicting major and by-products using electronic and structural effects. The arrow push mechanism must be shown.(19, 8, 3) Specify a synthetic scheme that would produce the compound shown above in the fewest steps possible. Use one of the starting materials shown together with any of the available reagents. Give the number of the starting material followed by the letters of the reagents in the order of their use, for example: 3be.A difficult problem in the synthesis of PGF2α is the introduction of the OH group at C15 in the desired configuration. a. Label this stereogenic center as R or S. b. A well known synthesis of PGF2α involves reaction of A with Zn(BH4)2, a metal hydride reagent similar in reactivity to NaBH4, to form two isomeric products, B and C. Draw their structures and indicate their stereochemical relationship. c. Suggest a reagent to convert A to the single stereoisomer X.
- We are currently working with diastereomeric products of acid-base reactions in my organic chemistry class and while I understand the basics of the creation of selectively soluble salt products, drawing the reactions has always been difficult. Our prelab asks us to "draw the expected diasteromeric products from the reaction of racemic phenylsuccinic acid with excess (s)-methylbenzylamine and label the chiral centers" I would really appreciate some help with this!A difficult problem in the synthesis of PGF2α is the introduction of the OH group at C15 in the desired conguration.a. Label this stereogenic center as R or S.b. A well known synthesis of PGF2α involves reaction of A with Zn(BH4)2, a metal hydride reagent similar in reactivity to NaBH4, to form two isomeric products, B and C. Draw their structures and indicate their stereochemical relationship.c. Suggest a reagent to convert A to the single stereoisomer X.After E2 elimination, will the following molecule contain deuterium? Why or why not?
- A student was given from the list of the compounds below A, B and D blindly and asked to identify them all. He treated each of them with Brady's reagent (2,4-ditrophenylhydrazine) and isolated a bright yellow compound for one of them, but the other two gave false negatives. The student reasoned that the false negatives may be due to sterics and, on further thinking, it dawned on him that he might be able to rule out one of the false negatives with the haloform test. What compound did he find compatible with the haloform test? That compound did indeed give a false negative in the Brady test. Which of the other two was positive in the Brady test? A = haloform B = Brady A = haloform D = Brady B = haloform A = Brady B = haloform D = Brady D = haloform A = Brady D = haloform B = BradyShow an actual arrow-pushing mechanism for the transformation below, and briefly explain the observed regioselectivity.A difficult problem in the synthesis of PGF2α is the introduction of the OH group at C15 in the desired configuration. a. Label this stereogenic center as R or S. b. A well-known synthesis of PGF2α involves reaction of A with Zn(BH4)2, a metal hydride reagent similar in reactivity to NaBH4, to form two isomeric products, B and C. Draw their structures and indicate their stereochemical relationship. d. Suggest a reagent to convert A to the single stereoisomer X.
- we know that ethers, such as diethyl ether and tetrahydrofuran, are quite resistant to the action of dilute acids and require hot concentrated HI or HBr for cleavage. However, acetals in which two ether groups are linked to the same carbon undergo hydrolysis readily, even in dilute aqueous acid. How do you account for this marked difference in chemical reactivity toward dilute aqueous acid between ethers and acetals?Show the electron-flow mechanism of the synthetic schemes (Aniline) of the picture below. This involves predicting major and by-products using electronic and structural effects. The arrow push mechanism must be shown.Which is the major organic product of the sequence below?