The correct answer is the 3rd option Ductility is a property of a metal. It is the ability of a material to deform under tensile stress.It is characterized by the ability to be stretched into wire-like form which is an ability of metals.
Answer:
Option A.
2Na + 2H2O —> 2NaOH + H2
Explanation:
To know which option is correct, we shall do a head count of the number of atoms present on both side to see which of them is balanced. This is illustrated below below:
For Option A:
2Na + 2H2O —> 2NaOH + H2
Reactant >>>>>>> Product
2 Na >>>>>>>>>>> 2 Na
4 H >>>>>>>>>>>> 4 H
2 O >>>>>>>>>>>> 2 O
Thus, the above equation is balanced.
For Option B:
2Na + 2H2O —> NaOH + H2
Reactant >>>>>>> Product
2 Na >>>>>>>>>>> 1 Na
4 H >>>>>>>>>>>> 3 H
2 O >>>>>>>>>>>> 1 O
Thus, the above equation is not balanced.
For Option C:
2Na + H2O —> 2NaOH + H2
Reactant >>>>>>> Product
2 Na >>>>>>>>>>> 2 Na
2 H >>>>>>>>>>>> 4 H
1 O >>>>>>>>>>>> 2 O
Thus, the above equation is not balanced.
For Option D:
Na + 2H2O —> NaOH + 2H2
Reactant >>>>>>> Product
1 Na >>>>>>>>>>> 1 Na
4 H >>>>>>>>>>>> 5 H
2 O >>>>>>>>>>>> 1 O
Thus, the above equation is not balanced.
From the illustrations made above, only option A is balanced.
You should always do A. form a hypothesis before performing an experiment also the other options cannot happen until after an experiment.
Answer:
Balanced equation have equal number of atoms of different elements in the side of reactants and products.
Answer:
The carbocation intermediate reacts with a nucleophile to form the addition product.
Explanation:
The reaction of benzene with an electrophile is an electrophillic substitution reaction. Here the electrophile replaces hydrogen. There is no formation of carbocation as intermediate in the reaction. Infact there is transition state where the electorphile attacks on benzene ring and at the same time the hydrogen gets removed from the benzene. So a transition carbocation is formed.
The general mechanism is shown in the figure.
i) Attack of the electrophile on the benzene (which is the nucleophile)
ii) The carbocation intermediate loses a proton from the carbon bonded to the electrophile.
iii) the carbocation formation is the rate determining step.
iv) There is no formation of addition product.
Thus the wrong statement is
The carbocation intermediate reacts with a nucleophile to form the addition product.
