Answer:
Phenols do not exhibit the same pka values as other alcohols;
They are generally more acidic.
Using the knowledge that hydrogen acidity is directly related to the stability of the anion formed, explain why phenol is more acidic than cyclohexane.
Explanation:
According to Bromsted=Lowry acid-base theory,
an acid is a substance that can release 
ions when dissolved in water.
So, acid is a proton donor.
If the conjugate base of an acid is more stable then, that acid is a strong acid.
In the case of phenol,
the phenoxide ion formed is stabilized by resonance.
The resonance in phenoxide ion is shown below:
Whereas in the case of cyclohexanol resonance is not possible.
So, cyclohexanol is a weak acid compared to phenol.
Answer:
A physical property is any property that is measurable, whose value describes a state of a physical system.
Explanation:
-color
-density
-volume
The balanced equation that illustrates the reaction is:
2C4H6 + 11O2 ......> 8CO2 + 6H2O
number of moles = mass / molar mass
number of moles of oxygen = 2.1 / 32 = 0.065625 moles
Now, from the balanced equation, we can note that:
11 moles of oxygen are required to produce 6 moles of water.
Therefore:
0.065625 moles of oxygen will produce:
(0.065625*6) / 11 = 0.03579 moles of water
number of moles = mass / molar mass
mass = number of moles * molar mass
mass of water = 0.03579 * 18 = 0.644 grams
Answer:
Temperature is the condition of the atmosphere at any given time and place
and climate is the weather over a long period of time
Explanation:
I think so-
The reduction of alkyne to an alkene in the first step allows the best reagent to be chosen for each subsequent step.
Describe reagents.
A reagent is merely an essential component of a chemical reaction, it should be mentioned. It is an ingredient that speeds up the reaction.
With H2 and Lindlar's catalyst, an alkyne is reduced to alkene as the initial step in this process. Alkene will then be brominated to produce allyl bromide as the next step.
In this instance, the required allyl alcohol will be produced via the reaction of allyl bromide with NaOH.
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