Is Sulfuric Acid a hydroxylic or polar aprotic solvent?
In Sulfuric Acid, which is a better nucleophile? Cl- or Br-? Why?
And is DMSO a hydroxylic or polar aprotic solvent?
In DMSO, which is the better nucleophile? Cl- or Br-? Why?
Is Sulfuric Acid a hydroxylic or polar aprotic solvent? In Sulfuric Acid, which is a better...
Oorai Which is the better leaving group in protic solvent? 1. Which is the better leaving group in aprotic solvent? I or Cl 2. Which is stronger base? I or Cl 3. Which is the stronger nucleophile in protic solvent? I or Cl 4. or CI Which is the stronger nucleophile in aprotic solvent? 5. Which is the stronger nucleophile? HO or H2N 6. 7. Which ion the better leaving group? CH,O or CH3CO2 Oorai Which is the better leaving...
13. Consider the nucleophiles, F, Cl, Br, and I. In a polar, aprotic solvent, which should be most reactive? WHY? (2) 14. Consider the nucleophiles, F', Cl, Br, and I. In a polar, protic solvent, which should be most reactive? WHY? (2)
In a polar aprotic solvent, which nucleophile will be more reactive? H2O or OH- I know that in a protic solvent its OH- but is it the opposite from polar aprotic?
which reagent in each pair would be the more reactive nucleophile in polar aprotic solvent? a pdl apohe dt a) He Nue vs. MeNH vs. ADe keoH V9 J) фом V9 Кзое f)NH3 NH VS. Awchons -Br
12. Which is not a polar aprotic solvent? A) C) 0 D) I CH: CH E) 13. Which is a polar aprotic solvent? A) 2-methylhexane B) CCl C) NH I) D) CH CH CH OCH C CH E) 2-methy 1-2-propanol
Which is NOT a polar aprotic solvent? (A)acetone (B) acetonitrile (C)DMF (D)methanol
О С OD Questions DMSO is a compound often used as a polar aprotic solvent. Analyzing formal charge, what is the formal charge on sulphur? a) -2 20 HC-S-CHE d) оо B с Question 6 MacBook Air
42) Which of the following is an example of polar, aprotic solvent? a. hexane C. carbon tetrachloride b. acetone d. ethanol 43) Which of the following is the best leaving group? OH b. OCH d. H0
8. Which of the following is a polar aprotic solvent? OH CH₃ A. CH3CHCH; B. H- N C. CH2CH2CH2CH2CH3 CH; D. HOCH CH2CH2CH3 E. None of the choices are correct.
just circle the answer Why do you think polar aprotic solvents increase the rate of an SN2 reaction? a) Polar solvents dissolve the substrates most effectively, speeding up the reaction b) Aprotic solvents better solvate the leaving group and therefore accelerate the reaction c) Aprotic solvents solvate the nucleophile less, 'naked' nucleophiles are more reactive d) Aprotic solvents raise the enegy of the reagents and therefore accelerate the reaction