Gaining electrons would mean that it is near the stable octet, so it needs more.
Right side would be the answer
Answer:
(a) 156.41 (b) 10 and 14 (c) 16
Explanation:
The question is incomplete, the complete question is shown in the image attached
Answer:
A and B
Explanation:
The electrophilic substitution of arenes yields a cation intermediate. The positive charge of the cation is delocalized over the entire ring.
The -CN group directs incoming electrophiles to the ortho/para position. The resonance structures for the chlorination of benzonitrile are shown in the question.
Recall that -CN is an electron withdrawing group. The resonance forms that destablize the carbocation intermediate are those in which the -CN group is directly attached to the carbon atom bearing the positive charge as in structures A and B.
Answer:
CCl4 - Nonpolar
CH3OH - polar
NH3 - polar
CS2 - Nonpolar
Explanation:
One important thing that we should know is that polarity has to do with the presence of a resultant dipole moment in a molecule.
Dipole moment is a vector quantity, This means that its direction is also taken into account when discussing the dipole moment of molecules.
Hence, symmetrical molecules such as CS2 and CCl4 are non-polar even though they have polar bonds because their dipoles cancel out(zero resultant dipole moment).
On the other hand, NH3 and CH3OH are non-symmetrical molecules hence they possess an overall dipole moment and are polar molecules.
Balanced equation = 2 NaHCO3 —-> Na2CO3 + H2O + CO2
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