Answer:
CH3CHO+H2O → CH3OCH3 - addition
CH,CICH CI + Zn → C2H4 + ZnCl2 - elimination
CH3CH3Br + OH – CH3CH3OH + Br - substitution
2CH2COOH >>(CH3CO)20 + H20 - condensation
Explanation:
An addition reaction is a reaction in which a specie is added across the double bond as we can see in CH3CHO+H2O → CH3OCH3.
In an elimination reaction, a small molecule is lost from a saturated compound to form the corresponding unsaturated compound as in CH,CICH CI + Zn → C2H4 + ZnCl2
In a substitution reaction, a chemical moiety replaces another in a molecule as in; CH3CH3Br + OH – CH3CH3OH + Br .
A condensation reaction is in which two molecules are joined together to form a bigger molecule as in; 2CH2COOH >>(CH3CO)20 + H20.
It's the second one. Their body activity decreases, mostly because they're sleeping and they conserve the food in their bodies for long periods of time.
<span>the marmots' body activity decreases to conserve food stored in their bodies.</span>
Answer:
I don't know
Explanation:
Maybe they shouldn't copy each other
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.
