Explain why an amide ion cannot be used to form a carbanion from an alkane in a reaction that favors products. explain why an amide ion cannot be used to form a carbanion from an alkane in a reaction that favors products. the base that would be formed is a weaker base than the alkane (the reactant base). the base that would be formed is a stronger base than the alkane (the reactant base). the acid that would be formed is a stronger acid than the alkane (the reactant acid).
Answers: 1
Chemistry, 22.06.2019 05:30
Describe the interaction that occurs between two objects with the same electrical charge.
Answers: 1
Chemistry, 22.06.2019 13:30
Which of the following has wavelength longer than the wavelength of viable light? a) x rays b) gamma rays c) radios waves d) ultraviolet waves
Answers: 1
Chemistry, 22.06.2019 14:30
For the reaction shown, find the limiting reactant for each of the following initial amounts of reactants. 4al(s)+3o2(g)â2al2o3(s) a) 1 molal, 1 mol o2 b) 4 molal, 2.6 mol o2 c) 16 molal, 13 mol o2 d) 7.4 molal, 6.5 mol o2
Answers: 3
Explain why an amide ion cannot be used to form a carbanion from an alkane in a reaction that favors...
Mathematics, 10.11.2020 06:40
Mathematics, 10.11.2020 06:40
Mathematics, 10.11.2020 06:40
Mathematics, 10.11.2020 06:40
Mathematics, 10.11.2020 06:40
Mathematics, 10.11.2020 06:40
Health, 10.11.2020 06:40
English, 10.11.2020 06:40
Mathematics, 10.11.2020 06:40
Biology, 10.11.2020 06:40