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...
Look un n-butyl bromide. Assume that this alkyl halide was prepared instead of the chloride. Decide weather the alkyl halide would appear as the upper or the lower in the conical vial when washing with cold water. ( what is the density of the n-butyl bromide?)
7, (10) Give the alkyl halide which would give only the alkene shown by way of an E2 elimination (one alkyl halide for each alkene):
when an alkyl halide undergoes E2 elimination the halogen and leaving hydrogen must be/have 21. When an alkyl halide undergoes E2 elimination the halogen and leaving hydrogen must be/have A. moni on the same carbon parallel bonds anti-periplanar a low activation energy none of these
Which alkyl halide would be most reactive in an SNI reaction? III Select one: b. 11 C. HII d. IV e. V
Which alkyl halide would you expect to react more rapidly by and SN2 mechanism? Why? 1 which alkyl halide would you expect to eact nou rapidly by an Su2 mechanism? Why? a) n. Pribor vs. t-Bu Br b) i- Buch vs. n-Buch c) Lacive. ya
Which of the following alkyl halide will not undergo Sul or Sn2 reaction?
1. Write the general equation for the reaction of an alkyl halide (RX, where R = alkyl group and X = halide) with AgNO3 in ethanol. Indicate which product will precipitate out of solution. 2. Write the general equation for the reaction of an alkyl halide (RX, where R = alkyl group and X = halide) with Nal in acetone. Indicate which product will precipitate out of solution. 3. Draw a complete reaction mechanism using the curved-arrow notation for each...
21. When an alkyl halide undergoes E2 elimination the halogen and leaving hydrogen must be/have A B. on the same carbon parallel bonds anti-periplanar a low activation energy none of these யே SN2 reactions work best with? polar aprotic solvents tertiary alkyl halides weak nucleophiles polar protic solvents none of these யே
Which of the following alkyl halide will not undergo SN1 or SN2 reaction? PA