The correct chemical formulae is CsBr
Democritus was the first to propose the idea of the atom. He said the atom was just this tiny, solid sphere. However, he used no scientific evidence to support his claim, so a guy named John Dalton did some experimenting and basically backed up Democritus' claim with evidence. Then, a guy named J.J. Thompson came along and said the atom was not solid and that is consisted of tiny negatively charged particles(electrons) and he came up with the Plum Pudding model which is just a tiny sphere with a punch of random scattered dots in it. After that, Ernest Rutherford did experiments and found that the tiny sphere is made up of mostly empty space with a tiny, dense, positively charged sphere inside of it, and the negatively charged particles just randomly float around it. Neils Bohr then said that the electrons take specific, circular, evenly spaced paths. Then, finally, we come to the Quantum Mechanical Model which is the one accepted today. This model basically vetos Bohr's idea and has a nucleus inside of an electron cloud, which is where the electrons are found.
Given:
n = 12 moles of oxygen
T = 273 K, temperature
p = 75 kPa, pressure
Use the ideal gas law, given by
where
V = volume
R = 8.3145 J/(mol-K), the gas constant
Therefore,
Answer: 0.363 m³
Answer:1:En química, el número másico o número de masa es la suma del número de protones y el número de neutrones del núcleo de un átomo. Se simboliza con la letra A (el uso de esta letra proviene de alemán Atomgewicht, que quiere decir peso atómico, aunque sean conceptos distintos que no deben confundirse).
2:
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.
