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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:
8.4
Explanation:
-log(4.08x10^-9) = 8.4
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Answer: An atom with 6 protons, 5 electrons, and 7 neutrons
Explanation: In this case, neutrons do not matter as they have a charge of 0, or no charge. A proton has a charge of +1 and an electron has a charge of -1. Since there are 6 protons, the total charge of the protons would be +6. Since there are 5 electrons the total charge of the electrons would be -5. +6 - 5 would result in a charge of +1. This means that this atom would have an overall charge of + 1. Basically, if there is one more proton than electron, then the overall charge of the atom will be +1 but if there is one more electron than proton, then the overall charge of the atom will be -1.