Answer:
With Br2 - Bromobenzene
With Cl2 - Chlorobenzene
With HNO3- Nitrobenzene
With H2SO4 - Benzenesulphonic acid
With HCOCl - Benzoyl chloride
With 1-chloro-2,2-dimethylpropane - 2,2dimethyl-1-phenyl propane
Explanation:
The common thread joining all these reactions is that they are all electrophillic reactions. They are so called because the attacking agents in each reagent is an electrophile. Electrophiles are species that have electron deficient centers and are known to attack molecules that are high in electron density at regions of high electron density.
The benzene molecule has rich electron density. Any substituents that donates electrons to the ring improves the likelihood that benzene will undergo electrophillic substitution reactions while electron withdrawing substituents decrease the likelihood that benzene will undergo electrophillic substitution reactions.
The names of the compounds formed when benzene undergoes electrophillic reaction with the attacking agents listed in the question are displayed in the answer section.
im not sure about this one but i think the field is spread out
Answer:
Electrons move around a nucleus.
Explanation:
Answer:
0.500 mol/dm³
Explanation:
Using the formula below;
CaVa = CbVb
Where;
Ca = concentration of acid (mol/dm³)
Cb = concentration of base (mol/dm³)
Va = volume of acid (cm³)
Vb = volume of base (cm³)
In accordance to the information provided in this question is;
Va = 5cm³
Vb = 250 cm³
Ca = 12 mol/dm³
Cb = ?
Using CaVa = CbVb
12 × 5 = Cb × 250
60 = 120Cb
Cb = 60/120
Cb = 0.500 mol/dm³
That's a ketone's functional group :)
