SN1 and SN2 Reactions - Page 2
Questions
- What is a substituent in organic chemistry?
- Why is sn2 concerted?
- Why does SN2 favor aprotic?
- How does concentration affect SN1 reactions?
- Why do SN2 reactions prefer aprotic solvents?
- What are common mistakes students make with nucleophilic substitutions?
- Is stereochemistry destroyed by #S_(N)1# reactions...?
- What is the effect of leaving group and solvent on the reaction rate of #S_N2# reaction?
- How does temperature affect SN1 reactions?
- What are SN1 and SN2 reactions?
- What affects SN2 reaction rates?
- Would 2-chloropropane or 1-chloro-2,2-dimethylpropane undergo substitution faster with #"HC≡C"^-"#, #"Na"^+#?
- How can I recognize #"S"_N1# reactions?
- Why is acetone used in SN2 reactions?
- What conditions favour nucleophilic substitution?
- How does temperature affect SN1 and SN2 reactions?
- Why is it good to do SN2 reactions in polar aprotic solvents?
- What is the SN2 reaction mechanism?
- How does concentration affect SN2 reactions?
- How are SN1 reactions solved?