Oxymercuration of 3-methylcyclopentene rightarrow (A) 1-hydroxy-2-methylcyclopentane + 1-hydroxy-3-melhylcyclopentene (B) 1-hydroxy-2-methylcyclopentane + 1-hydroxy-5-methylcyclopentene (C) 1 -hydroxy-3-methylcyclopentane +...
1. Draw the following molecules, based on their IUPAC name: a) 2-hydroxy-5, 5-dimethylheptanedioic acid; b) 3-hydroxy-7-methylnonanedioic acid 2. Give the IUPAC name for the following compounds: A) HO OH 3. Circle the name that is correct for each molecule, based on IUPAC rules. V a) 4-methylheptanoate 4-methylbutanoate b) pentyl 4-metylhexanoate c) 3-methylbutyl 4-methylhexanoate d) isobutyl 4-methylhexanoate
Question 1 ( --/1) Reaction of 6-bromo-2-methyl-2-heptene with hydrogen on Pd/C will provide which product? 1 6-bromo-2-methylheptane 2 2-methyl-6 bromoheptane 3 2-bromo-6-methylheptane © 2-bromo-6-methylhexane We were unable to transcribe this imageQuestion 3 ( -- / 1 Given the reaction of 3-methylcyclopentene witih NBS and light, what is one possible product? 1 3-bromo-3-methylcyclopentene (2) 5-bromo-5-methylcyclpentene 3 3-bromo-3-methylcyclopentane 4-bromo-3-methylcyclopentene
11. What is the product of this reaction? acetone A) 2-hydroxy-2-methylpropanoic acid B) 2-cyano-2-propanol C) 1-amino-2-hydroxy-2-methylpropane D) 2-hydroxy-2-methylbutanoic acid E) none of the above 1) HCN 2) H20/4+ / heat
Q43 43. What is the IUPAC of the following compound? HO A) 5-Hydroxy-3-methyl-1-pentene B) 3-Methyl-5-penten-1-ol C) D) 3-Methyl-1-penten-5-ol 3-Methyl-4-penten-1-ol ta vield a carbocation that is
Question 11 4 pts Predict the starting material for this reaction. HS (18,3S)-3-methylcyclopentane-1-thiol (15,35-1-iodo-3-methylcyclopentane (1R 3R)-1-iodo-3-methylcyclopentane (1R 3S)-1-iodo-3-methylcyclopentane (15,3R)-1-iodo-3-methylcyclopentane
Select the IR spectrum that corresponds best with 3-hydroxy-2-butanone. a) b) c) d)
Please help with 3 a,b ,c,d 2. Acid catalyzed hydration and oxymercuration-demercuration of an alkene, both add water in a Markovnikov fashion. What are some advantages for the latter process. 3. Predict the major product(s) of the following reactions and provide a mechanism; a. 1-methylcyclohexene + HBr b. 1-methyl-1-cyclopentene + H O. CH CH OH c. 1-pentyne + HBr d. 1,3-butadiene + HBr
Please give 4 steps to making 3-methylcyclopentene from 1-methylcyclopentene. Drawing should be provided with mechanism.
ОН. Provide a name for the molecule shown. A 3-iodo-5-isopropoxyphenol B meta-iodo meta-isopropoxyphenol С 1-isopropoxy-3-hydroxy-5-iodocyclohexane D 5-iodo-3-isopropoxyphenol E 5-iodo-3-isopropoxycyclohexanol F 1-hydroxy-3-iodo-5-isopropoxycyclohexane G 3-iodo-5-isopropoxycyclohexanol
C_aH_s + 6O_2 rightarrow 4 CO_2 + 4 H_2 O b) C + 2 H_2 rightarrow CH_4 c) 4 Cu + 4 HNO_3 rightarrow Cu(NO_3)_2 + 2 NO_2 + 2 H_2 O