NOSJE 1) LIOM, MOH 2) 0.1 M aq. H,SO 2) 0.1 M aq. H SO LIOME MeOH, 65°C excess Bra NaOH HBr 1) NaH, DMF, OC 2 3) H SOHO
Please provide the major organic product(s) of the reaction as
described. Account for all stereochemistry requirements for
reaction and products. You need not include byproducts such as
salts for this assignment, but you should be aware of their
presence. "No reaction" is NOT a possibility on this
assignment.
1) LIOMe, MeOH 2) 0.1 M aq. H2SO4 2) 0.1 M aq. H2SO4 LIOMe MeOH, 65'C excess Br2 NaOH HBr 1) NaH, DMF, O C 2) 3) H2SO4 H20
Please provide the major organic product(s) of the reaction as
described. Account for all stereochemistry requirements for
reaction and products.
excess Br2 NaOH HBr 1) NaH, DMF, O C 2) 8 3) H2SO4, H2O
Lab 11 Acid-Base Titration Part 2: Data Table for H2SO, titration HSO4 (aq) + 2 NaOH(aq) Table 3. Data + Sulfuric Acid Volume Na2SO. (aq) + 2 H2O(1) used - 10.00 m2 - Trial 1 Trial 2 Trial 3 (optional) H2SO4 used (A, B, C) Actual volume of H2SO4 (mL.) Initial buret reading (mL) Final buret reading (mL) 2.52mL 1.50mL 19.40mL 14.6ImL 31.42 m2 19.50ml Table 4. Results Calculations Trial 1 Trial 2 Trial 3 (optional) Volume of NaOH nitrated...
From the following list, determine the missing reagents.
a. NaOH. b. Hz, Pd/C C. NaOH, H202 d. NaoMe, MeOH e. Na, NH3 f. H2SO4 H20 g. NaNH2 h. CrO2, H2SO4 (aq) 1. NaBH4, MeOH H2SO4, MeOH k. C PK I. Met m. Phli n. H2, Lindlar's catalyst O. BH3, THE p. Nah q. H30+ workup r. PCC s. OsO4, H2O2 t 03. -78 °C - H - K
QUESTION 9 Using the list, propose the forward synthesis of the retrosynthesis shown below (and number of steps can be used, so long as they get to the desired product in as high a regioselectivity as possible). Please report your answer by typing the letters/symbols sequentially. A. Ph3PMeBr, KotBu, PhMe, 25 °C B. CuBr, 0 °C C. Cu20, Cu(NO3)2, H20, 0 °C D. CuCN, 0 °C E. SO3, H2SO4, 100 °C F. Cl2, FeCl3, THF, 65 °C G. Br2, FeBr3,...
Using the list, propose the forward synthesis of the retrosynthesis shown below (and number of steps can be used, so long as they get to the desired product in as high a regioselectivity as possible). Please report your answer by typing the letters/symbols sequentially. A. Ph3PMeBr, KotBu, PhMe, 25 °C B. CuBr, 0 °C C. Cu20, Cu(NO3)2, H20, 0 °C D. CuCN, 0 °C E. SO3, H2SO4, 100 °C F. Cl2, FeCl3, THF, 65 °C G. Br2, FeBr3, THF, 65...
Please provide the major organic product(s) of the reaction as
described. Account for all stereochemistry requirements for
reaction and products.
1) LiOMe, MeOH 2) 0.1 M aq. H2SO4 1) Eto 2) 0.1 Maq. H2SO4 LIOME اما « MeOH, 65°C
1) A flask containing 450.0 mL of 0.500 M HBr was spilled on
the floor. How many grams of K2CO3 would you need to put on the
spill to neutralize the acid according to the following
reaction?
2 HBr (aq) + K2CO3 (s) => 2KBr (aq) + H2O (l)
2) Determine the molarity of an unknown NaOH solution if 25.00
mL of sodium hydroxide was titrated with 15.00 mL of a 1.500 M
sulfiric acid solution (H2SO4). (aOH= 40.00 g/mol...
Choose the sequence of reagents which would best accomplish the following transformation: 2-bromopropane ----------> 1,2-dibromopropane [(R) + (S)] 01. (i) KMnO4, NaOH in water at 0 °C 2. (i) Br2 in CCl4 (ii) excess NaNH2 (iii) CH31 (iv) H20, H2SO4, HgSO4 Choose the sequence of reagents which would best accomplish the following transformation: 2-bromopropane ---------> 1,2-dibromopropane [(R) + (S)] 01. (i) KMnO4, NaOH in water at 0 °C 2. (i) Br2 in CC14 (ii) excess NaNH2 (iii) CH3 (iv) H20,...