When energy is added to a system during phase change, the particles move faster.
When a substance is heated, the internal energy within a system associated with the motion of particles and that can be added to a substance is called thermal energy.
During a phase change, when more energy is added to the system, the particles within the system will have greater motion and the temperature will increase.
The attractions that hold molecules together are electrostatic forces. The correct statement about the attractions that hold particles is that attractions between particles break when attractions due to Electrostatic forces when particles move fast enough these forces can no longer keep particles together.
Rubber band is not a perfect comprehension for Bonds in a substance when considering phases change because for a phase change from liquid to gas the bonds do not break completely the particles can still slide past each other.
The pair of samples that will have the same average kinetic energy of benzene molecules is a sample of liquid benzene at 80°C and a sample of gaseous benzene at 80°C.
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Eutrophication
In an aged aquatic habitat like a lake, eutrophication is the progressive rise in the concentration of phosphorus, nitrogen, and other plant nutrients. As the volume of organic matter that can be converted into nutrients increases, the productivity or fertility of such an ecosystem also naturally rises.
<h3>What is Eutrophication ?</h3>
Eutrophication may be caused by a number of things, including overuse of fertilisers, untreated sewage, the use of phosphorous-containing detergents, and industrial waste discharge.
- Eutrophication naturally. Natural eutrophication is a process that develops in water resources over a very long period of time as a result of a slow buildup of nutrients and organic waste. Anthropogenic or cultural eutrophication.
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Answer:
None of these
Explanation:
Friedel–Craft reaction is a reaction involves the attachment of substituents to the benzene ring.
Mechanism of the reaction of methylbenzene with 1-chlorodecane in the presence of ether and aluminum chloride :
Step -1 : Generation of stable carbocation.
Aluminium chloride acts as Lewis acid which removes the chloride ion from the alkyl halide forming carbocation. The primary carbocation thus formed gets rearranged to secondary primary carbocation which is more stable due to hyperconjugation.
Step-2: Attack of the ring to the carbocation
The pi electrons of the ring behave as a nucleophile and attacks the carbocation. Since, the group attached on the benzene is methyl (+R effect) , the attack is from the ortho and the para positions. Para product is more stable due to less steric hinderance.
The product formed is shown in mechanism does not mention in any of the options.
So, None of these is the answer
I think it's A. because the Earth won't always have the same tilt throughout it's whole life. The tilt of the axis will change, even if it's just ever so slightly. I hope this helps and i hope i'm right :)