Answer:
Mutualism
Explanation:
A relationship in which both benefit
So we know the number of moles of each compound. If we need to know the concentration we must know the number of moles that the compounds react with...
Answer:
The four resonance structures of the phenoxide ion are shown in the image attached
The conjugate base of cyclohexanol has only one resonance contributor, while
the conjugate base of phenol has four resonance contributors.
Explanation:
In organic chemistry, it is known that structures are more stable if they possess more resonance contributors. The greater the number of contributing canonical structures, the more stable the organic specie. Since the phenoxide ion has four contributing canonical structures, it is quite much more stable than cyclohexanol having only one contributing structure to its conjugate base. Hence the PKa(acid dissociation constant) of phenol is lesser than that of cyclohexanol. The conjugate base of phenol is stabilized by resonance.
Answer:
The answer is 2,3-dimethylbutan-2-ol and the structure is attached below.
Explanation:
Although we are not provided with ¹H-NMR spectrum and IR spectrum but still we can elucidate the ¹³C-NMR data and finalize a plausible structure.
First of all we look at the molecular formula, we can conclude from the formula that the structure given is saturated in nature because the hydrogen deficiency index of this formula is zero. Hence, we can say that there is no double bond either between Carbon atoms or between carbon and oxygen atom. This can also be proved by the absence of peaks in downfield as unsaturated compounds and carbonyl compounds give value above 100 and 200 ppm respectively.
Secondly, we can also conclude that among the six carbon atom two pairs of them are having same electronic environment because we are having only 4 signals hence we can conclude that two pairs have same chemical shift values.
Also, after making every possinble isomer of given molecular formula the structure of 2,3-dimethylbutan-2-ol was found to be the most accurate structure.