Answer:
The classification and illustrations are attached in the drawing.
Explanation:
It is possible to identify the pure substance observing the figure, since it is the only one that has 2 joined atoms (purple and blue) which forms a single compound.
On the other hand, the homogeneous mixture is identified by noting that its atoms are more united with respect to the heterogeneous mixture, highlighting that in homogenous mixtures the atoms, elements or substances are not visible to the naked eye and are in a single phase, instead in the heterogeneous mixture if they can be differentiated.
Answer:
V= 12mL
Explanation:
you had the right idea with your Significant figures however, when we divide we see that it requires 2 significant figures as our least amount. this is because when looking at our division, 62 has 2 sig. fig. while 5.35 has a total 3. when looking at your answer we see that you had a total of 3 sig. figures. so in actuakity you had to round up to 12 and not to the tenths because the decimal makes .6 count as your third sig fig.
Answer:
For deposition to happen, thermal energy must be removed from the gas. ... As water vapor loses thermal energy, it changes into solid frost. States of Water. Water is the only substance that exists naturally as a solid, a liquid, and a gas within Earth's temperature range.
Explanation:
Answer:
Gases and particles in Earth's atmosphere scatter sunlight in all directions. Blue light is scattered more than other colors because it travels as shorter, smaller waves. This is why we see a blue sky most of the time.
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.
