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Answer:
Explanation:
Ketcher 01232019462D 1 1.00000 0.00000 0 5 4 0 0 0 999 V2000 -0.0330 2.2250 0.0000 C 0 0 0 0 0 0 0 0 0 0 0.8330 2.7250 0.0000 C 0 0 0 0 0 0 0 0 0 0 1.6990 2.2250 0.0000 C 0 0 0 0 0 0 0 0 0 0 0.8330 3.7250 0.0000 C 0 0 0 0 0 0 0 0 0 0 1.6990 1.2250 0.0000 C 0 0 0 0 0 0 0 0 0 0 1 2 1 0 0 0 2 3 1 0 0 0 2 4 1 0 0 0 3 5 1 0 0 0 M END
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:
A
Explanation:
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put 8 in front of the oxygen in the reactants side to make it 16 molecules then put a 5 in front of the co2 in the product side to balance the carbon atoms then put a 6 in front of the H20 on the product side this balances both the hydrogen and oxygen atoms here is a representation
C5H12(g)+8O2(g)=5CO2(g)+6H20