Answer:
The correct choice is E (47 neutrons, 35 protons, 36 electrons)
Explanation:
A ion of net charge -1 means that the ion wins an e-.
We dismiss options B and C.
We also dismiss option A because neutrons + protons = 81.
neutrons + protons = mass number
So we have E and C.
We see that C has 47 neutrons, 36 protons and 36 electrons and, as the atomic number matches the number of protons, we find out on the Periodic Table that the atomic number 36 represents to Krypton, a noble gas. It is impossible! A noble gas never can't be a ion of net charge.
Option E is correct, It is an isotope of Br.
Br has 35 protons (its atomic number)
47 neutrons, that's why it is an Isotope (Br has always 45 neutrons)
As usual, Br has 35 electrons, if it represents a ion of net charge -1, it menas it won 1 e-.
Hey there!
Molar mass N2 = 28.01 g/mol
Therefore:
28.01 g N2 -------------- 6.02*10²² molecules N2
( mass N2 ?? ) ----------- 25,000 molecules N2
mass N2 = ( 25,000 * 28.01 ) / ( 6.02*10²³ )
mass N2 = 700250 / 6.02*10²³
mass N2 = 1.163*10⁻¹⁸ g
Hope that helps!
D is the correct answer
every other option contains an element
<u>Answer:</u> The mass percent of hydrogen in methyl acetate is 8 %
<u>Explanation:</u>
The given chemical formula of methyl acetate is 
To calculate the mass percentage of hydrogen in methyl acetate, we use the equation:

Mass of hydrogen = (6 × 1) = 6 g
Mass of methyl acetate = [(3 × 12) + (6 × 1) + (2 × 16)] = 74 g
Putting values in above equation, we get:

Hence, the mass percent of hydrogen in methyl acetate is 8 %
Answer:
four (4)
Explanation:
Naphthalein is an organic compound with formula C
10H
8. It is the simplest polycyclic aromatic hydrocarbon, and is a white crystalline solid with a characteristic odor that is detectable at concentrations as low as 0.08 ppm by mass. As an aromatic hydrocarbon, naphthalene's structure consists of a fused pair of benzene rings. It is best known as the main ingredient of traditional mothballs.
The molecule is planar, like benzene. Unlike benzene, the carbon–carbon bonds in naphthalene are not of the same length. The bonds C1−C2, C3−C4, C5−C6 and C7−C8 are about 1.37 Å (137 pm) in length, whereas the other carbon–carbon bonds are about 1.42 Å (142 pm) long. This difference, established by X-ray diffraction is consistent with the valence bond model in naphthalene and in particular, with the theorem of cross-conjugation. This theorem would describe naphthalene as an aromatic benzene unit bonded to a diene but not extensively conjugated to it (at least in the ground state), which is consistent with two of its three resonance structures.
Because of this resonance, the molecule has bilateral symmetry across the plane of the shared carbon pair, as well as across the plane that bisects bonds C2-C3 and C6-C7, and across the plane of the carbon atoms. Thus there are two sets of equivalent hydrogen atoms: the alpha positions, numbered 1, 4, 5, and 8, and the beta positions, 2, 3, 6, and 7. Two isomers are then possible for mono-substituted naphthalenes, corresponding to substitution at an alpha or beta position. Bicyclo[6.2.0]decapentaene is a structural isomer with a fused 4–8 ring system.
Therefore four (4) double bonds will be added to give each carbon atom an octet structure.