Introduction to Reactions and Mechanisms - Page 5
Questions
- How does a Diels Alder reaction work?
- What does ozonolysis do?
- How do you represent the loss of carbon dioxide from soda lime, #Na_2CO_3#?
- How will you prepare propanamine from methyl chloride using suitable reactions?
- Why does furan undergo Diels Alder reaction?
- What are alkanes, alkenes, and alkynes?
- How do you get ethanoic acid from ethyne gas?
- Conversion Methanol to tertiary butyl cyanide?
- What is the action of 4-methylphenylhydrazine on a carbonyl group, with reaction and example?
- How does propane react with bromine under radical conditions?
- How will you convert methane to the following: (a) propane (b) butane (c) methyl butanoate (d) ethanoic acid (e) ethanol?
- Why do you add hexanes (after toluene) in the recrystallization of the adduct in a Diels-Alder reaction?
- When an adduct is formed from Diels Alder reaction of maleic anhydride and furan, what does the adduct decompose to at its melting point?
- Can anyone help me with these mechanisms for the formation of spiro heterocycles?
- How could you improve the yield of diels alder reactions?
- How do you differentiate between free radical, nucleophile, electrophile, carbocation and carbanion?
- What will be product(s) if ethylene glycol is treated with fuming sulphuric acid & heat ?
- What is a dehydration reaction with respect to alcohols?
- Why are alkenes more reactive than other functional groups?
- Why alkenes called olefins?