There are eight bonded electrons in this molecule! :)
Answer:
Al ascender las burbujas van aumentando de tamaño.
Explanation:
Las burbujas que produce el buzo debajo del agua son pequeñas moléculas de dióxido de carbono gaseoso producto de la respiración del mismo.
Ahora, a medida que las burbujas suben a la superficie, la presión que sufren estas (Presión debido al agua), es menor conforme van ascendiendo debido a la ley de Boyle: A medida que la presión aumenta, el volumen va disminuyendo.
Esto significa que al ascender las burbujas van aumentando de tamaño debido a que la presión que sufren estas es menor que cuando están a mayores profundidades.
Answer:
325mg of Aspririn
Explanation:
First you should note the information that the problem gives you:
- The bottle of Aspirin has 5gr (grains)
- 1gr(grain) = 65mg (miligrams)
Also, the problem is asking about how many aspirin are in 5 gr (grains), so you should use a conversion factor, as follows:
-First you should put the quantity you need to convert:

-Then you write the denominator of the conversion factor that must have the same units that you want to convert, in this case gr:

-Then you write the numerator with the units that you want to obtain and the numerical equivalence between the units, in this case:

-Finally you multiply numerators and divide by denominators:

The question is incomplete. Complete question is attached below
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Correct Answer:
Option C i.e. I ~ III < IV < V < II
Reason:
During a nucleophilic subsitution reaction of chloroarenes, Cl- group is replaced by an nucleophile like OH-.
Order of reactivity, during such reactions depends on the electron density on carbon atom that is attached to Cl. Lower the electron density, greater will be the reactivity.Among the provided chloroarenes, electron density on C atom will be minimum in case of compound II, because of presence of electron withdrawing group (-NO2) at ortho and para position. Due to this, there will be large number of resonating structures. This signifies greater electron de-localization, and hence largest reactivity for nucleophilic substitution reaction.
Followed by this, compound V will show greater reactivity, due to presence of -NO2 group at para and one of the ortho position. Compound IV will have less number of resonating structures as compared to compound II and V, hence it will display poor reactivity towards nucleophilic substitution reaction.
Finally, compound 1 and III will minimum reactivity towards nucleophilic substitution reaction, because -NO2 group present at meta position (compound III) will not participate in resonance.