Answer:
Nitrobenzene is too deactivated (by the nitro group) to undergo a Friedel-Crafts alkylation.
Explanation:
The benzene ring in itself does not easily undergo electrophilic substitution reaction. Some groups activate or deactivate the benzene ring towards electrophilic substitution reactions.
-NO2 ia a highly deactivating substituent therefore, Friedel-Crafts alkylation of nitrobenzene does not take place under any conditions.
This reaction scheme is therefore flawed because Nitrobenzene is too deactivated (by the nitro group) to undergo a Friedel-Crafts alkylation.
Answer:
Solid Osmium transition metal reacts with Oxygen gas to produce solid Osmium tetroxide.
Os(s) + 2O₂(g) -> OsO₄(s)
Explanation:
Osmium tetroxide is another way of writing Osmium (VIII) oxide.
Leaving powdered osmium exposed to air in a room will slowly create osmium tetroxide at room temperature.
Similarly, osmium tetroxide vapor will readily be released from a liquid solution at room temperature.
Answer:
Its long wire narrow wire more resistance
Explanation:
I took the same k12 test
Answer:
Kinetic energy would have to work ten times harder than potential energy.
Explanation:
Let’s say you have a boulder and your asked to push it up the hill it would be difficult right? But lets reverse the situation what if you are asked to roll the boulder down the hill it wouldn’t be much work because the hill is basically doing all the work For you. Hope this Helps:)