1.
Application of EA2. [HYDROCARBONS REVISION] Electrophilic Addition
Feature of carbon-containing intermediates formed via FRS and EA.3. [HYDROCARBONS REVISION] Electrophilic Addition
Which is the correct energy profile diagram?4. [HYDROCARBONS REVISION] Electrophilic Addition
Which is the major carbocation intermediate formed?5. [HYDROCARBONS REVISION] Electrophilic Addition
Rate of EA based on stability of carbocation intermediate.6. [HYDROCARBONS REVISION] Electrophilic Addition
Which are the major and minor products?7. [HYDROCARBONS REVISION] Electrophilic Addition
Applying Markovnikov’s Rule to find the number of chiral carbons formed in the major product.8. [HYDROCARBONS REVISION] Electrophilic Addition
Applying Markovnikov’s Rule to find the major product.9. [HYDROCARBONS REVISION] Electrophilic Addition
Which compound is not formed from the reaction of ethene with aqueous bromine in the presence of sodium chloride?10. [HYDROCARBONS REVISION] Electrophilic Addition
Applying Markovnikov’s Rule to find the major product.11. [HYDROCARBONS REVISION] Electrophilic Addition
When cyclohex-1,4-diene is treated with a solution of Br2 in CCl4, what is the product formed? Are there enantiomers and can the product mixture rotate plane-polarised light?12. [HYDROCARBONS REVISION] Electrophilic Addition
How many chiral centers does the product have?13. [HYDROCARBONS REVISION] Electrophilic Addition
Which pair of compounds are formed from the reaction of ethene with aqueous bromine in the presence of sodium chloride?