Answer:
Time allowed for incubation, size of the dish, the amount of light, amount of agar, the type of agar…etc
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.
261.162 grams. Use the equation n=M÷Mr.
The balanced chemical
reaction will be:
C4H8 + 6 O2 --> 4 CO2 + 4 H2O
We are given the amount of butene being combusted. This will be our
starting point.
136.6 g C4H8 (1 mol C4H8/ 56.11 g C4H8) (4 mol CO2/1 mol <span>C4H8</span>) ( 44.01 g CO2/ 1 mol CO2) = 428.6 g CO2