PLEASE HELP ME. I DO NOT
UNDERSTAND
PLEASE HELP ME. I DO NOT UNDERSTAND a. b. +HIO4 c. + H+ Pd/C H2+Pd/C d....
please explain
How can this transformation be accomplished? OTS ?, A. Bry/CCI: B. H./Pd-C c. O/CHOH D. Br /HO H.B-H G. H.0 /acid I. H.O/NaOH F.H.O E. Zn K. NaH J. CI/H0 L. mCPBA M. H.SOJA N. TsCl/py 0. KMnO/KOH [A] H then M P. NaOH [B] D Q. HO/H.SO [C] O [D] P then B [E] K Explanation for your choice (3 pts)
please show the mechanisms for d-i
Chapter 14: Carboxylic Acids Please Show Reaction mechanisms (d) 1. H.Cro 1. BH3 2. H,O, HO Na o 2. NaOH NaOH e) H2 OH ОН CH,COOH H Pt 1. BH; HACO () HO 2. H.O., NaOH SOCI HO O R R RCI Cl2 HẠCrO4 19 AICI: AICI: OCH OH CH,OH H RCI used in the first reaction cannot be a tertiary alkyl halide. (h) heat ОН OH H2CO (1) OH 1. LAIH Lo La...
not real sure how to do H or K
Product(s) Reactants/conditions a. H2,Pt H2/Pd/BaSO4, quinoline Na/NH3 b. 2 eq, HCI H2SO4, HgSO4, H2O 1 eq, Cl2 2 eq. Cl2 1. NANH2 2. CH3CH2Br YR h. 1. Sia2BH/THF i. 2. H2O2/OH j. KMnO4, H2O KMnO4, NAOH NANH2, NH3 H2, Pd H2/Pd/BaSO4, quinoline k. I. m. n. Na/NH3 о. 2 eq, HCI p.
Help on Organic Chemistry homework
HCrO4 A B FeClh AICly H2 Pd/C E AICI Zn(Ha HC G F AICI Cl N,H OH H FeCl Br FeB J K H-SO Cн-Clz L AICI 2 moles Br M FeBr3
A. i) Ho^ OH, TOH, Dean-Stark; ii) Pd/C, H2; iii) EtBr; iv) H2O, HCI B. i) 2 EVOH, TOH, Dean-Stark; ii) a) MeLi, b) EtBr; iii) H2O, HCl; iv) Pd/C, H, C. i) excess EtOH, H2SO4, heat; ii) a) MeMgBr, b) EtBr; iii) Pd/C, Hz; iv) H.O, HCI D. A and C would both work E. B and C would both work
Hello, can you please help me out with these problems. Thanks in
advance.
What reagents and conditions produce this transformation? 58. OH steps (A) 1. H2, Pd/C 3. NaOH, H2CO 4. NaBH4, CH3OH 5. Нзо", (CH3)2CO (B) 1. H2, Pd/C 2. NaBH4, CH OH 3. NaOH, Н.СО 4. pyridine-HCICrOs (PCC) 5. Нзо", (CH3)2CO (C) 1·Hao", (CH3)2CO 2. H Cros, H2S04, H2O 3. CH3MgBr 4. CHsCoH So2Cl (TsCl) 5. H2, Pd/C (D) 1. 1,3-butadiene, heat 2. H2, Pd/C 3. SOC12, pyridine...
Question 44 (a,b,d,f,i) and 46 (a,c,e,f)
please, I don't understand.
Give the expected major product of the reaction of propyne with each of the following reagents. (a) D_2, Pd-CaCO_3, Pb(O_2CCH)_2, quinoline: (b) Na, ND_3: (c) 1 equivalent HI: (d) 2 equivalents HI: (e) 1 equivalent Br_2: (f) 1 equivalent ICl: (g) 2 equivalent ICl: (h) H_2O, HgSO_4, H_2SO_4: (i) dicyclohexylborane, then NaOH, H_2O_2 What are the products of the reactions of dicyclohexylethyne with the reagents in Problem 44? Write the...
Please help! This is due soon and I don't understand it.
A. How would I separate F and G?
B. How would I separate G. and H.?
Separation Options are:
1. suction or gravity filtration
2. aq. NaOH/diethyl ether extraction
3. aq. NaHCO3/diethyl ether extraction
4. silica gel column chromatography
5. evaporation under reduced pressure
6. water/diethyl ether extraction
7. aq. HCL / diethyl ether extraction
OH CI b.p. 302 od b.p. 332 °C
Please help me with problem B. Please provide details
to help me understand.
B. Titration of an Antacid Description Antacid 1 Antacid 2 Brand of Antacid Tums Alka-Seltzer Bases( s) in Antacid CaCO NaHCO; Mass of Flask 178.64g 178.55g Mass of Flask and Antacid 179.11g 178.93g Molarity of HCI Solution 0.10M 0.10M Total Volume (mL) of HCL Solution Added 500ml 50.Om Molarity of NaOH Solution 0.10M 0.10M Initial Volume (mL) of NaOH Solution 0.54ml 0.58ml Final Volume (mL) of NaOH...
Predict the Products. Can you please show it step by step. It
will help me understand more. Thank you in advance
2. D2 CH3CH2-C=C-CH3 Indy 3 Lindlar catalyst -C=C-H 1.BH, THF 2.H20, NaOH, H2O KMnO4 H20+ 5. CH3CH2C=CH HgSO4, H2SO4 Н20