
Chemistry
10th Edition
ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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Transcribed Image Text:18. Provide the mechanism for the catalytic hydrogenation reaction shown below.
H₂
Pt
X
H₂
H
(+ entantiomer)
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- Complete the followsing reactionse a. CH20H + CH3 CHz_ott Ho Cit2OH CHO otH +Cu+ CH20H CH3 + Cltz CH -OH HF OHarrow_forwardComplete the given reactions by drawing the structures of the major organic products: Please draw the completed reaction OH HO HOCN H₂N H₂O H3PO4 OH HO HO. (excess) H3O+ H2SO4 H*arrow_forwardWhat reagent)(s) would accomplish the conversion shown below? ? cat. OsO4, H202 Ozone, then (CH3)3S RCO3H H2O2, NaOHarrow_forward
- 1. Cl2, H20 2. NaOH Another mechanism for the formation of epoxides is through the formation of a chlorohydrin. Alkenes react with chlorine in the presence of H,0 to give a chlorohydrin via a cyclic chloronium ion intermediate. When the chlorohydrin is treated with strong base, HCl is eliminated and the epoxide is formed. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructionsarrow_forwardto 1. conc. HBr H20 Br OH O Na 2. Na NH2 NH3 d = El Elimination f = SN1 Nucleophilic substitution a = Proton transfer b = Lewis acid/base e = E2 Elimination g = SN2 Nucleophilic substitution c = Electrophilic addition The rections above involve synthesis or reactions of alcohols and ethers. Identify the mechanism by which they proceed from among the mechanisms listed. Use the letters a - g for your answers. 1. 2. Submit Answer Retry Entire Group 8 more group attempts remainingarrow_forwardClassify each of the following species as a nucleophile or an electrophile CH3 CH3-CECH CH3- -CH3 O:c EN: CH3-0-CH3 | I II III IVarrow_forward
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