Answer:
I'll give you the graphs that you need to look at:1st order: the graph you need to make is ln[A] vs t. If you get a straight line, the reaction is 1st order and the slope will equal to the rate constant K.2nd order: the graph you need to make is 1/ln[A] vs t. If this graph shows a straight line, the reaction is 2nd order and the slope will equal the rate constant K.
Explanation:
<u>Answer:</u>
<em>The amount of energy needed when water at 72 degrees c freezes completely at 0 degrees c is
Joules</em>
<em></em>
<u>Explanation:</u>

where
= Final T - Initial T

=30125J
Q is the heat energy in Joules
c is the specific heat capacity (for water 1.0 cal/(g℃)) or 4.184 J/(g℃)
m is the mass of water
mass of water is assumed as 100 g (since not mentioned)
is the heat energy required for the phase change
=mass × heat of fusion

Total heat =
Total Heat = 30123J + 33600J
= 63725 J
=
Joules is the answer
We find the weight of the empirical formula:
12.0107 + 2 x 1.00794 + 15.9994
= 30.03
Now, we divide the molecular weight by the weight of the empirical formula to find the number of times the empirical formula repeats:
90.09 / 30.03
= 3
The formula is 3(CH₂O)
C₃H₆O₃
1) Chemical formula for propane is CH₃-CH₂-CH₃.
Propane is a three carbon alkane (acyclic saturated <span>hydrocarbon).
</span>2) Chemical formula for propanal is CH₃-CH₂-CH=O.
Propanal <span> is a </span>saturated<span> three carbon </span>aldehyde (have<span> a </span>carbonyl<span> center).
3) </span>Chemical formula for propanol is CH₃-CH₂-CH₂-OH.
1-propanol <span> is a </span><span>primary alcohol.
4) </span>Chemical formula for propanone is (CH₃)₂-C=O.
Propanone or acetone is <span>he simplest and smallest</span> ketone.
Answer:
Explanation:
Structure of the 2,2,4,4-tetramethyl-3-pentanone is give in the attachment
In 2,2,4,4-tetramethyl-3-pentanone, no alpha hydrogen is present, therefore, enol form is not possible and hence, exist only in keto form.
Explanation for existence of cyclohexa-2,4-diene-1-one only in enol form:
keto form of cyclohexa-2,4-diene-1-one not aromatic and hence less stable.
Whereas enol form it is aromatic which makes it highly stable. that's why cyclohexa-2,4-diene-1-one exists only in enol form.