All explanation is given below structures of some polar protic
solvent is give in explanation
why Sn2 reactions will not work with polar protic solvents? draw structures to explain if possible...
Write the mechanism of the following substitution reaction Explain why Polar protic solvents favor SN1 reactions. Do you expect this substrate to react under SN1. explain your answer.
I think the Nucleophilicity of the leaving material on polar protic solvents that It is the opposite with the basicity (because nucleophilicity increase down a column) Is it true that Basicity opposites the nucleophility in polar protic solvents? I think that when comparing the nucleophilicity of CH3COO- CH3CH2O- The CH3CH2O- is bulky compared to CH3COO- so I think the CH3CH2O- would be less nucleophilic but the answer says the CH3COO- is less nucleophilic because it is less basic. I wonder...
questions 7. Why are polar protic solvents preferred for Syl reactions? A. Solvent ionizability B. Hydrogen bonding C.Heat Capacity D.Both A and B E.Both B and C ene chloride)? 8. Why is triflate (A) a better leaving group then tosylate (B) OSICF В A A. Atomic Size B. Resonance C. Hybridization D.Polarizability E. Inductive Effects E 9. Which compound is the stronger Base? A. Lithium Hydroxide B. Sodium Acetate C. Triethyl amine D. Potassium tert-butoxide E. Water 10. What is...
Problem 3: Identify each of the following solvents as polar protic or polar aprotic. poiar Polar polar pronic oprotic polar Drotis, Ho Polar polar polar pronc opronic Piotic
Sodium borohydride reductions are typically run in polar protic solvents such as methanol or water. Vanillin is only sparingly soluble in water or methanol, thus for this reaction vanillin was dissolved in 1.0 M NaOH (aq). Explain with the use of a reaction mechanism why vanillin is more soluble in 1.0 M NaOH than water. [2.0 Marks]
7&8 please
7. True or False: Iodide is the best nucleophile in polar protic and polar aprotic solvents. 8. Select the alkyl halide that would be expected to undergo the fastest E2 reaction. or yor yor
explain why a polar protic solvent speeds the rate of an SN1 mechanism
3. The nucleophilicty of ionic nucleophiles (like SH- or alkoxides) can change dramatically from polar protic solvents to polar aprotic solvents. On the other hand, the nucleophilicty of neutral, molecular nucleophiles (like H2S, or neutral alcohols ROH) remains relatively constant in both types of solvent. Explain these differences using examples of both types of nucleophiles interacting with common protic and aprotic solvents.
3. The nucleophilicty of ionic nucleophiles (like SH- or alkoxides) can change dramatically from polar protic solvents to polar aprotic solvents. On the other hand, the nucleophilicty of neutral, molecular nucleophiles (like H2S, or neutral alcohols ROH) remains relatively constant in both types of solvent. Explain these differences using examples of both types of nucleophiles interacting with common protic and aprotic solvents.
I need help with 1-4 please
Question 1: Find a table that compares the relative reaction rates (Su2) for alkyi fluorides, chlorides, bromides and iodides (Section 9.2 in the textbook). Which halide is the best leaving group? How much faster is it than the slowest halide leaving group? Question 2: The nature of the solvent plays a big role in determining the type of substitution or elimination mechanism that takes place (SH1, SN2, E1 or E2). Draw structures for 2...