Answer:
As electro-negativity decreases from Florine to downwards in the group and only Florine is above Chlorine, so Florine should react with sodium chloride solution to produce chlorine.
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Explanation:
By<em> </em><em>drilling</em><em> </em><em>several</em><em> </em><em>cores</em><em> </em><em>miles</em><em> </em><em>ap</em><em>art</em><em> </em><em>,</em><em> </em><em>geologist</em><em> </em><em>c</em><em>a</em><em>n</em><em> </em><em>correlate</em><em> </em><em>the</em><em> </em><em>rock</em><em> </em><em>units</em><em> </em><em>and</em><em> </em><em>create</em><em> </em><em>an</em><em> </em><em>image</em><em> </em><em> </em><em>what</em><em> </em><em>exists</em><em> </em><em>and</em><em> </em><em>where</em><em> </em><em>below</em><em> </em><em>the</em><em> </em><em>surfac</em><em>e</em><em>.</em>
<em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em>
<em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em>Combining</em><em> </em><em>this</em><em> </em><em>information</em><em> </em><em>with</em><em> </em><em>rocks</em><em> </em><em>exposed</em><em> </em><em>to</em><em> </em><em>the</em><em> </em><em>surface</em><em> </em><em>,</em><em> </em><em>which</em><em> </em><em>can</em><em> </em><em>gives</em><em> </em><em>clues</em><em> </em><em>about</em><em> </em><em>rock</em><em> </em><em>orientation</em><em> </em><em>below</em><em>,</em><em> </em><em>can</em><em> </em><em>be</em><em> </em><em>a</em><em> </em><em>powerful</em><em> </em><em>tool</em><em> </em><em>to</em><em> </em><em>locating</em><em> </em><em>oil</em><em> </em><em>and</em><em> </em><em>gas</em><em> </em><em>.</em>
Acid palmitic acid has higher melting point, because it has two more methylene groups.

Acid palmitic acid has higher melting point, because it has two more methylene groups.
Giving it a greater surface area and therefore more intermolecular van der waals interact than the myristic acid.
stearic arid 
linoleic acid
(two double bond)
Stearic acid has higher Melting point, because it does not have any Carbon-Carbon double bonds, whereas linoleic acid has two cis double bonds which prevent the molecules from packing closely together.
Oleic Acid and Linoleic acid.
-one double bond (cis)
Acid palmitic acid has higher melting point, because it has two more methylene groups.
For more such question on methylene group.
brainly.com/question/4279223
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Answer:
b) The dehydrated sample absorbed moisture after heating
Explanation:
a) Strong initial heating caused some of the hydrate sample to splatter out.
This will result in a higher percent of water than the real one, because you assume in the calculation that the splattered sample was only water (which in not true).
b) The dehydrated sample absorbed moisture after heating.
Usually inorganic salts may absorbed moisture from the atmosphere so this will explain the 13% difference between calculated water percent the real content of water in the hydrate.
c) The amount of the hydrate sample used was too small.
It will create some errors but they do not create a difference of 13% difference as stated in the problem.
d) The crucible was not heated to constant mass before use.
Here the error is small.
e) Excess heating caused the dehydrated sample to decompose.
Usually the inorganic compounds are stable in the temperature range of this kind of experiments. If you have an organic compound which retain water molecules you may decompose the sample forming volatile compounds which will leave crucible so the error will be quite high.
The answer is long wave length because long wave lengths contians less energy, and would not harm living things such as plants and animals. the more engey a wave length has, the less harmful it is.
short wave length: lots of energy, extremely hot. (examples: gamma rays, and UV (ultraviolet) rays.
long wave lengths: not much energy, safe for humans and other life on Earth.
hopefully this helps.