He encontrado que alguna farmacia puede tener existencias limitadas de ciertos medicamentos, mientras que otras pueden tener casi cualquier formato que se le ocurra y el habitual de dosis habitualidad apareció. En resumen, siempre se contiene el almacén de corroborar. Al mismo tiempo que el producto que más que gustaba ha resultado no estaba disponible en stock otro distinto por las Buenas costumbres también debe buscarse jefe no asн parezca. Por eso es importante disponer de un Plan B para actuar cuandod ello no ocurra. Ventaja de tomar un genérico en lugar de Asix Un genérico es más barato que el nombre de marca Uno de los mayores incentivos para someterse al Dónde comprar Lasix genérico en lugar de pagar la marca es que usted puede obtener un ahorrando importantes Lasix genérico. Por lo tanto, un Lasix genérico es en general mucho más barato que el homólogo de marca, así que una denominación genérica se hace posible para las personas que usan este medicamento con frecuencia. Un ejemplo: La compra de lurosemida en lugar de Lasix es una considerable ahorro para el presupuesto mensual de medicamentos.

Microsoft word - s08ex1key.doc

Organic Chemistry II
KEY
February 14, 2008
1. Which of the following starting material/ reagent combinations would give rise to chlomiphene, a fertility agent? E
2. The major kinetic product(s) of the reaction of 2-methyl-2-pentene with Cl2, H2O is (are): A
a)
Organic Chemistry II
KEY
February 14, 2008

3. The major product of the reaction below is: B
4. Phase I metabolism of the anti-histamine, triprolidene involves an epoxidation process, similar to the reaction of trans- 2-butene with p-chlorobperbenzoic acid. The epoxide
metabolite(s) of triprolidine would be expected to be: B
a) a single stereoisomer b) a racemic mixture c) a mixture of only two diastereomers d) a mixture of multiple stereoisomers (enantiomers and 5. Which of the following alkenes would provide 1-bromo-1-methylcyclopentane as the major kinetic product upon reaction with HBr without going through a rearrangement? C
a) I b) II c) I & II d) III & IV e) I, II, III, IV Organic Chemistry II
KEY
February 14, 2008
6. Which of the following kinetically-controlled reactions will provide a racemic mixture as the major products? A
7. Selegiline, an anti-histamine agent provides a ketone when reacted with aqueous acid and an aldehyde when reacted with 1) BH3 and 2) H2O2, NaOH, H2O. Reaction with one
equivalent of HCl gives a single product but reaction with one equivalent of Cl2 provides a
mixture of stereoisomers. Which of the following structures represents selegiline? C
Organic Chemistry II
KEY
February 14, 2008
8. Which of the following reaction intermediates is involved in the preparation of tramadol, an analgesic, from treatment of the alkene (given below) with aqueous acid? A
9. Which set of reaction conditions will provide the product shown as the only product of the
reaction? A
10. Treatment of 1-methylcylobutene with 1) HgCl2, cyclobutanol and 2) NaBH4 will provide: Organic Chemistry II
KEY
February 14, 2008
11. Which of the following alcohols will give methysticin the fastest upon treatment with 12. Which of the following alkenes will provide both of the products, A and B when reacted with Organic Chemistry II
KEY
February 14, 2008
13. Which of the following reaction intermediates gives rise to the major kinetic product of the reaction below? D
14. The carbonyl group of oxefedrine, an antianginal agent, is derived from which of the following enols? D

15. Which of the following compounds can undergo E2 elimination? C
Organic Chemistry II
KEY
February 14, 2008
16. Which of the following epoxides will give two ketone products when reacted with acid? (Assume no rearrangements occur) D
17. Reaction of compound I with sulfuric acid (no water) under thermodynamic conditions gives compound II. Compound A (not a reaction intermediate) is generated from I and then goes
on to react to give compound II. Which structure(s) represent(s) “A”? D
18. Rank the stability of the reaction intermediates below from most stable to least stable (most>>least) B
a) II > I > > IV > III b) II > IV > I > III c) II > IV = I > III d) I =IV > II > III e) I = II > IV > III Organic Chemistry II
KEY
February 14, 2008

19. Which of the following reaction energy diagrams correspond to the reaction given below? D
20. Conversion of 2-methyl-2-butene to 2-methoxy-2-methylbutane can be accomplished with:
D
a)
Organic Chemistry II
KEY
February 14, 2008


Questions 21-25:
Matching column: Match the reactions (questions 21-25) with the appropriate set of
reagents (choices a-e). Each reagent may be used once, more than once or not at all.
a) AcOH b) AcOH, H2O c) 1. m-ClPBA 2. AcOH d) 1. HgCl2, H2O 2. NaBH4
21. E
22. E
23. B
24. A
25. C

Source: http://organicchem.org/oc2web/lecture/exams/S2008/s08ex1key.pdf