Answer:
See explanation.
Explanation:
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In this case, according to the given information, it turns out possible for us to firstly recall the electron configuration of hydrogen:
To realize that the principal quantum number is 1, the angular is 0 as well as the magnetic one; therefore we infer that all the given n's are not allowed, just l=0 is allowed as well as ml=0 yet the rest, are not allowed.
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Answer:
4. trigonal planar symmetry.
Explanation:
The sp2 hybridization is formed with one s and two p atomic orbitals and form trigonal planar symmetry. In sp2 hybridization, there are same valence shell in both the orbitals and it gives three equivalent sp2 hybridized orbitals that are separated by 120 degrees giving trigonal planar symmetry.
Hence, the correct answer is "4. trigonal planar symmetry.".
Answer: See below
Explanation: a. The mass of an element is composed of:
protons: 1 amu each
neutrons: 1 amu each
electrons: 0 amu each
Only the protons and neutrons are counted in the atomic mass of an element
b. Electrons are assigned a mass of 0. They do have a mass, but it is exceedingly small compared to the protons and neutrons, so they are left out of the calculation of an element's mass.
c. An element becomes unstable if the neutrons exceed the protons by a certain ratio, dependent on the element.
Answer:
a, g, c
Explanation:
The conversion of the stable cyclopentane into Trans-1, 2dibromocyclopentane will require three step reactions.
The first is to convert the compound into a cyclopentene, through the addition of Bromine water under heat and photons (light). So option A is the first in the order. This will generate 1 bromocyclopentane through halogenation of the alkane. Secondly, a hot and strong base should be added like the NaOEt, EtOH to remove the added bromine and one atom of hydrogen from the resulting 1 bromocyclopentane in the previous reaction. This will yield cyclopentene, thus making the compound more electrophilic. So option g is required. Thirdly, bromine molecules will be added (C) to take up their places at the two electrophilic regions of the compound to produce Trans-1, 2dibromocyclopentane.
