31.
In the presence of light energy C - C bond gets cleaved homolytically, to give two methyl radicals.
The way you wrote is correct.
32.
The way of movement of pi electrons through homolytic cleavage to give the different resonance structure is correct.
33.
Addition of bromine radical to pi bond leads to more stabel tertiaru carbon free radical, that you have drawn is correct.
34.
The steps that do not involve in the formation of active radicals indicate the termination steps.
(c)
(d)
are the termination reactions.
Note: All your answers are correct.
are my answers okay? 3. Use correct arrow formalism to show a bomolytic bond cleavage of...
Ho for the pre c! . Given the bond dissociation energies below in Kcal/mol, estimate the ano forth (CH),CH-CI step . CHCI c) 40 kcal/mol (CH.J.CH a) +22 kcal/mol b)-22 kcal/mol e) -45 kcal/mol he major monobrominated product that results from when methylcyclopentane is subjected d) +45 kcal/mol c) a tertiary halide radical bromination is b) a secondary halide e) bromomethane a) A primary halide d) A quaternary halide 3. Which of the following is a termination a) Cl +...
help please 3. Used curved arrows to show the following: a) Homoly tic bond cleavage of a C-H bond in methane b) Homolytic bond clenvage of the Br--Br bond in Br c) Heterolytic bond cleavage of the HCI molecule C H Heterolytic bond cleavage of the O-H bond in CH O
pleas help 5,6,7,8,9,10 III IV 5. The product of free-radical halogenation reactions is an alkyl halide. The major amount of this halide forms during the second step of propagation. However, you should be aware that one possible termination step also forms alkyl halides. Why does the majority of the alkyl halide product come from the propagation step and not the termination step? A. At any given time during the reaction, the concentration of both the alkyl radical and the halide...
please help me with Organic Chemistry/Alkenes problems. Thank you! Directions: Place your answers to the following questions in the spaces provided. 1. A common problem in the acid-catalyzed hydration of alkenes is the formation of an ether byproduct. Show the formation of the ether byproduct in relation to the reaction below by providing a curved-arrow mechanism for its formation. (2 pts) H30+ Н,0 OH Ans. 2. Which is the correct sequence of steps necessary to complete the following reaction? он...