Advertisements
Advertisements
प्रश्न
Compare SN1 and SN2 reaction mechanisms.
उत्तर
SN1 | SN2 | |
Rate law | Unimolecular (Substrate only) | Biomolecular (substrate and nucleophile) |
“Big Barrier” | Carbocation stability | Steric hindrance |
Alkyl halide (electrophile) | 3° > 2° > 1° | 1° > 2° > 3° |
Nucleophile | Weak (generally neutral) | Strong (generally bearing a negative charge) |
Solvent | Polar protic (e.g., alcohols) | Polar aprotic (e.g., DMSO, acetone) |
Stereo Chemistry | Mix of retention and inversion | inversion |
APPEARS IN
संबंधित प्रश्न
Benzene reacts with Cl2 in the presence of FeCl3 and in absence of sunlight to form ______.
The most easily hydrolysed molecule under SN1 condition is ______.
Which one of the following is most reactive towards nucleophilic substitution reaction?
Silver propionate when refluxed with Bromine in carbon tetrachloride gives ______.
t – butyl chloride reacts with aqueous KOH by SN1 mechanism while n – butyl chloride reacts with SN2 mechanism.
Predict the products when Bromo ethane is treated with the following.
AgNO2
Write a short note on Dows Process.
Starting from CH3MgI, How will you prepare the following?
Ethyl acetate
Starting from CH3MgI, How will you prepare the following?
Iso propyl alcohol
Complete the following reaction.
\[\ce{CH3 - CH2 - Br + NaSH ->[alcohol][H2O]}\]