Introduction to Reactions and Mechanisms - Page 3
Questions
- How do you do addition reactions of alkenes?
- What happens in ozonolysis?
- What is electrophilic aromatic substitution?
- How can i dentify the nucleophile and the electrophile in #H-Br# + #HO^-)hArr Br^-#+#H_2O# acid–base reaction?
- What is the expected major product/products arising from the reaction of methylpropene with dilute potassium permanganate?
- Why is sulfide a better nucleophile than the structurally equivalent alkoxide?
- What makes ethanoic acid a weaker electrophile than ethanoyl chloride?
- How is #"propionic acid"#, #"H"_3"CCH"_2"CO"_2"H"#, synthesized?
- What is a dehydration reaction?
- Why is diethyl ether used to extract an organic product from water at the end of a reaction?
- How do you classify alkanes, alkenes and alkynes?
- Why does methanol (an alcohol) make methyl orange (an indicator) turn yellow?
- How do you convert Benzaldehyde to Benzophenone in exactly two steps?
- What is ozonolysis and its applications?
- Give the action of the Clemmensen reduction on 2-butenal?
- Write the equation for the preparation of a Grignard reagent using 2-bromo-3-methylbutane and name the alkane produced after its hydrolysis?
- Write the overall reaction for reaction of methyl benzoate with excess phenyl magnesium brimide in ether, followed by H3O+. ????
- How can you reverse ozonolysis?
- Why is #N_2O_5# not widely used as a laboratory reagent? On the other hand, why is #P_2O_5#, and #CaO#, and #H_2SO_4# widely used?
- How do alkenes react with bromine water?