Consider the compound A= 2 chloro 2 methy butane , B= 2 chloro butane, C= chloro propane. Which of the compound will readily undergo dehydrochlorination, what informs your answer? Expert's answer

The sequence of nucleotides in the template DNA strand strictly determines the sequence of nucleotides in the replicated DNA strand. The rigor of the construction of the nucleotides of the...

b)1-chloro-3-nitrobenzene

M(C3H8) = 44 g/moln(C3H8) = 5000 (g)/44 (g/mol) = 113,6 molN = n•NA = 113,6 • 6,02•1023 = 684,1•1023 molecules Answer: 684,1•1023 molecules of propane are in the cylinder.

1) CH3-CH2-CH2-CH3 + Cl2 ---gt; CH3-CH2-CH2-CH2-Cl + HCl CH3-CH2-CH2-CH2-Cl + KOH (dry) --gt; CH3-CH2-CH2=CH2 CH3-CH2-CH2=CH2 + Br2/H2O2 --gt; CH3-CH2-CH2-CH2-Br CH3-CH2-CH2-CH2-Br + KOH (aq) --gt; CH3-CH2-CH2-CH2-OH + KBr CH3-CH2-CH2-CH2-OH + NaBr/H2SO4...

The answer is compound A.If the mechanism of elimination is E1 then the reactivity of dehydrohalogenation is dependent on stability of carbocation. The more stable the carbocation the more readily...

Dehydrochlorination reaction proceeds most actively in the molecules with high numbers of substitutes around carbon atom which linked with a chlorine atom. Such structure makes final alkene molecule more stable...

2-chloro-2-methylbutane will readily undergoes dehydrochlorination, since it will form the most stable carbocation after elimination of chlorine atom.

2-chloro-2-methylpropane is more stable since it would form less stable carbocation upon elimination of chlorine, while phenylethyl carbocation is more stable due to the stabilisation of the positive charge by...

a)C6H12b) C6H11Cl3C)C9H16

According to Clausius Clapeyron equation:ln(P2/P1) = (-∆Hvap)/R × (1/T2 - 1/T1),where T1 - boiling point (-42°C = 315.15 K), T2 - temperature (25°C = 298.15 K), ∆Hvap - heat of...