The given solvents are classified into protic and aprotic based on their connectivity of the atoms.
The structure of all the solvents are drawn to check whether the hydrogen atom present in the solvent is bonded to an electronegative atom or not.
Electronegativity of an atom is defined as the property of an atom to attract the bonded electron pair towards itself.
Protic solvent is the solvent in which the hydrogen atom is attached to an electronegative element. The electronegative element can nitrogen, oxygen or fluorine.
These solvents contain active in their solutions. These solvents participate in hydrogen bonding in the reactions. They serve as acids.
Aprotic solvent is the solvent in which the hydrogen atom is not attached to an electronegative element.
These solvents do not contain active in their solutions. These solvents do not participate in hydrogen bonding in the reactions.
The protic solvents are the ones which have hydrogen atom attached to the electronegative atom.
The protic solvents are as follows:
The aprotic solvents are the ones which have hydrogen atom attached to the electronegative atom.
The aprotic solvents are as follows:
Ans:
The given solvents are classified into protic and aprotic solvents as follows:
Classify the following solvents as either protic or aprotic solvents.
18 Classify the following solvents as either protic or aprotic solvents. Note: If one or more solvents are incorrectly placed, a single red X will appear on the top left. Protic Aprotic DMF DMso acetonitrile acetone H20 cH3CH20H CH3OH acetic acid
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
Classify the following five solvents in each appropriate category. The dielectric constant (€) is provided for each solvent. 1. Ethanol (E=25) is a: O O polar solvent non-polar solvent protic solvent aprotic solvent O O donor solvent non-donor solvent 2. Dimethylformamide (E=37) is a: O O polar solvent non-polar solvent O O protic solvent aprotic solvent O O donor solvent non-donor solvent 3. Hexane (e=1.9) is a: O O polar solvent non-polar solvent O O protic solvent aprotic solvent O...
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
5. For each of the following solvents, provide an unambiguous structural formula. Then classify each solvent as protic, polar aprotic, or nonpolar. a. Ethanol b. Dimethylsulfoxide (DMSO) c. Hexamethylphosphoramide (HMPA) d. Benzene e. Heptane f. Acetic acid 9. Tetrahydrofuran (THF) h. Diethyl ether i Carbon tetrachloride j. Dichloromethane (DCM) k. Chloroform 1. Ethyl acetate
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.
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
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...
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...