Predict all organic products, showing stereochemistry where
appropriate
HBr (2) heat OH NaOH (3) H20 CH, CH3CH2OH (4). H H2SO4, 25 "C SNa
1. PCC CI 3. Cl2 H,0, heat 7- け 3. на, но 8- CH-CH HBr H20 refux 9- NH2 CH -C-Cl 10. 2.HaO кон. rMso 12- CH3 CH Ch 13- NH2 14- -78C 15- OH LiAIH 4 16- socl2 2 pyridine P2Os NH2 18- 1. NaHCO.. H2O 2. OH Br 19. 2, H30 20- 1. BH4 2. H3O 21- 22- 2. PBr 3.2 equiv. CH,CH CH&NH 23- 1. Mg Br 3. NaHCO Cl 24- 2 LAH 25-
What is the major product obtained from the following reaction sequence? Br2 EtONa NACN D HBr B A ETOH hv peroxides heat CN CN CN CN II III O A. III OB. IV O C.V OD II O E. I What would be the major product of the following reaction sequence? 1. HBr, ROOR, hv 2. CH CO-H, CH coNa OH 0.CCH 0.cCH Ph Ph I III IV O A.I O B. II O C. IV O D. II O...
predict the products of the following reactions
0 () CH,CH CCH,-C-OCH, NocCH (2) CH (3) Ho .heat (I) NaOCH2CH (2) H,O', heat (b) CH,-C-CH-C-OCH,CH,+ CH, (1) LDA -OH (c) Ph CH, () CH,CH,CH,Br (1) H2C-CH CH,Br (2) H0* OCH, NaOCH Ph (2) CH,CH,CH2CH2Br (g) product from part (f) (decarboxylation)
0 () CH,CH CCH,-C-OCH, NocCH (2) CH (3) Ho .heat (I) NaOCH2CH (2) H,O', heat (b) CH,-C-CH-C-OCH,CH,+ CH, (1) LDA -OH (c) Ph CH, () CH,CH,CH,Br (1) H2C-CH CH,Br (2) H0*...
(45 pts) What is the expected major product of the following.reaction sequence? 1 NacEL HOEt heat 2 HgrCAc) CH,OH 3 NaliH NaCH OCH3 OHH HyCO OCH3 IV- II II . (4.5 pts)Which is the correct sequence of reaction steps necessary to complete the following transformation? Br OH + enantiomer OH I. MCPBA II. NaOCH,CH. CH,CH,OH T. H,O" or -OH IV. 1) OsO, then 2) NaHSOH,O I then IV B) I then II then III C) II then I then III...
Question 3 (2 points) For the reaction shown, select the expected major organic product. 1. 1 eq HCI 2. 1 eq HBO Br -Br Br + enantiomer + enantiomer + enantiomer Br + enantiomer IV II a) 11 Ob) III O c) v Od) I Question 8 (2 points) What is the product of the reaction below? ТОН PCC O OH I II OH III IV a) 1 b) IV O c) III d) I Question 10 (2 points) Predict...
What is the IUPAC name of the given molecule? OH Br 1-bromo-2-ethyl-2-hydroxy-3-methylpentanoic acid 2-ethyl-3-methylpentan-2-ol-1-carboxyl bromide 2-ethyl-3-methyl-2-ol-pentanoyl bromide O2-ethyl-2-hydroxy-3-methylpentanoyl bromide What statement is TRUE about the mechanism for the reaction shown here? CH,(CH)2CO,CH, NaOH CH3(CH12COCH excess heat CH3(CH)2CO,CH2 Water attacks the carbonyl carbon to form a tetrahedral intermediate. The first step of the reaction involves protonation of the ester carbonyl oxygen. One of the products formed is glycerol. The hydroxide deprotonates the alpha carbon. Which bases among the following is/are used...
1. NaOEt CO2Et 2. H30+ 3. heat Br. Br CORET + H3C V CO2H H₂C + CO2 + E H3C CO2Et The malonic ester synthesis is a carbonyl alkylation reaction. It is used to prepare carboxylic acids from primary alkyl halides, lengthening the carbon In progress by two atoms. Thus, the product can be visualized as being a "substituted acetic acid." The reaction consists of three steps: generation of the enolate anion followed by SN 2 reaction with a primary...
Questions 2-10 please!!
1) A substitution reaction is: [2] a) A reaction during which an OH group of a molecule is replaced by a halogen. b) A reaction during which water is the leaving group. c) A reaction during which a functional group of a molecule is replaced by an electrophile. d) A reaction during which a functional group of a molecule is replaced by another functional group. V 12 2) Substitution reactions are classified either as electrophilic or nucleophilic...
i Running Times (in seconds) Country Heat <MUWLUI-YEZ Name Runner 1 Runner 2 Runner 3 Runner 4 Runner 5 Runner 6 Runner 7 Runner 8 Runner 9 Runner 10 Runner 11 Runner 12 Runner 13 Runner 14 con uno o o oNNNNNNN Time 51.13 51.94 52.02 52.03 52.45 52.84 54.59 51.49 51.82 51.96 51.98 52.24 52.69 53.71 Print Done In a certain running event, preliminary heats are determined by random draw, so it would be expected that the abilities of...