please help 15. Predict the product. Be sure to show stereochemistry OsO4 H2O2 mCPBA H2SO4 (aq)...
15. Predict the product. Be sure to show stereochemistry Os04 H202 mCPBA H2SO4 (aq) mCPBA 16. Draw out the complete mechanism for the chlorination of
WILL POSTIVE RATE CORRECT AND COMPLETE ANSWERS!!! Thanks! Predict the product(s) expected from the following reactions. Be sure to consider both the regiochemistry and the stereochemistry of the addition and if chirality centers are formed. Draw all stereoisomers produced. Predict the product(s) expected from the following reactions. Be sure to consider both the regiochemistry and the stereochemistry of the addition and if chirality centers are formed. Draw all stereoisomers produced. Br2 Cl2 Нао 1) MCPBA 2) Hао* 1) OsO4 2)...
please help with these reactions 12. What is the product? Pay attention to stereochemistry chlorin Cl2 Нао 13. Predict the product of these reactions: 93 1)BH3 THF 2) H2O2, -OH What H2SO4 17. D Н.о 14. Predict the product no reaction WHY? Br2 CH2Cl2 18. Br2 CH2CI2 show stereochemistry Br hv
Predict the major product(s) of the following reactions. Show stereochemistry where appropriate. 3 CO3H i) OsO4 H ii) NaHSO3, H2O CHC13, KOH any cha, kot i) BH3, THF CECH 11) H2O2, NaOH Li NH (liquid) cm X Ft, H/HO (vii) Two Markovnikov products Draw the structure of alkene for each of the following reactions. OH i) BH, THF 11) H202, NaOH 1) Hg(OAc)2, H20 ii) NaBH4 1) 03 ii) Zn/H Styrene undergoes propagation to give polystyrene. Showing electron-flow using half-headed...
Predict the major organic product or products of each of the following reactions: Identify the mechanism taking place in each of the reactions and please provide explanation. H2SO4 a) (CHỊ) CH CH=CH, HO Hg(OAc)2 NaBH4 b) (CH3)2CH CH=CH2 H2O BH3: THE H2O2, NaOH c) (CH3),CH CH=CH2 H2SO4, H2O d) CHCECH HgSO4 HZ/Ni f) + Cl2 + H2O g) Cold KMnO4 dilute h) 1. CH CO-OH 2. Hz0 Br2 i) CC14
Please help me!!! 17. (15) Draw the reaction occur Draw the major product or products of each of the following reactions indicate whether Ction occurs by an Syl,S2, E. or E, mechanism on the line provided. Be sure to include stereochemistry in your answers where it is appropriate OH a. mech: H2SO4 b. mech: - KOC(CH) HOC(CH3) c. mech: CH,CH,OH 40° KCN H20 d. mech: OH BI c. mech I Hot Cho con un Nal acetone (aq) 40 °C HC-CH2CH3...
1. Draw the structure of the principal organic product and predict the stereochemistry to be expected from the reaction of (IR, 2R)-/-bromo-2-methylcyclohexane with each of the following: a. NaOCH, in CH,OH at 60° d. NaNH, in NH, dt 50° b. aqueous CH OH at 140° e. aqueous CH.CH,OH at 25° c. Nal in DMSO at 40° 2. Draw the major product(s) (showing appropriate stereochemistry when necessary) for the following reactions. Indicate the mechanism(s) in operation (SNI,SN2, El. or E2). CH,...
please answer all 1. Draw the structure of the principal organic product and predict the stereochemistry to be expected from the reaction of (IR, 2R)-1-bromo-2-methylcyclohexane with each of the following: a. NaOCH, in CH,OH at 60° d. NaNH, in NH, at 50° b. aqueous CH,OH at 140° e. aqueous CH,CH,OH at 25° c. Nal in DMSO at 40° 2. Draw the major product(s) (showing appropriate stereochemistry when necessary) for the following reactions. Indicate the mechanism(s) in operation (SNI, SN2, E1,...
Name DIRECTIONS: You must complete the entire 1. PREDICT THE PRODUCT Provide the structure of the major product expected from the following reactions or reaction sequences. Make sure you want for any region or stereochemistry (24 p.) 1. HOOAC) CH OH 1) BH-THF 2) H20, KOH HBF, ROOR 1. BH-THF 2.HONOM H20, H2SO4 1. NaNH, H-CEC-CH2-CH2-CHE 2. CH,CHBr Lindlar cat 1. Sia BH-THF 2. H2O2, H20
1. (7 points) Draw the major, organic product generated for each of the reactions regiochemistry and stereochemistry. Be sure to indicate if more than one enantiomer is formed. below. Pay particular attention to the CI dilute H2SO4 KCN C2, H20 (dark) 1. BH3 THF 2. H2O2, KOH 1. NaH 2. allyl chloride (e) Draw the stereoisomer of 2,3-diphenylbut-2-ene that yields meso-2,3-dibromo-2,3-diphenylbutane on reaction with Br2 in the cold, darkness. 2.(2 points) Complete the following synthesis by filing in the missing...