Well a mixture is less permanent and also it can be easily taken aprt where a compound does the opposite of those things.
Hope I helped :)
Answer:
Approximately 10,5
Explanation:
The question is not really very specific, because it would need the percentages of those isotopes in the nature. As they are not shown, it should be the median of those two numbers.
atomic weight ≈ 
= 10,5
If you check a periodic table, you'll see it's actually 10,8, but that's because of the thing I told you at first (percentages missing).
Hope I could help.
Answer:
volume
v = 4/3π r^3
Explanation:
it isn't specific enough but that is the equation of how to get any volume
volume equals four thirds times pi times radios to the power of three
Answer : The amount of heat evolved by a reaction is, 4.81 kJ
Explanation :
Heat released by the reaction = Heat absorbed by the calorimeter + Heat absorbed by the water
![q=[q_1+q_2]](https://tex.z-dn.net/?f=q%3D%5Bq_1%2Bq_2%5D)
![q=[c_1\times \Delta T+m_2\times c_2\times \Delta T]](https://tex.z-dn.net/?f=q%3D%5Bc_1%5Ctimes%20%5CDelta%20T%2Bm_2%5Ctimes%20c_2%5Ctimes%20%5CDelta%20T%5D)
where,
q = heat released by the reaction
= heat absorbed by the calorimeter
= heat absorbed by the water
= specific heat of calorimeter = 
= specific heat of water = 
= mass of water = 254 g
= change in temperature = 
Now put all the given values in the above formula, we get:
![q=[(783J/^oC\times -2.28^oC)+(254g\times 4.184J/g^oC\times -2.28^oC)]](https://tex.z-dn.net/?f=q%3D%5B%28783J%2F%5EoC%5Ctimes%20-2.28%5EoC%29%2B%28254g%5Ctimes%204.184J%2Fg%5EoC%5Ctimes%20-2.28%5EoC%29%5D)
Therefore, the amount of heat evolved by a reaction is, 4.81 kJ
Answer:
Axial position
Explanation:
In the reduction of 4-tert-butylcyclohexanone with sodium borohydride, the major product has the tert-butyl group in the equatorial position and the alcohol in the axial position.
The reason for this is that, axial bonds are parallel to each other. If substituents are larger than hydrogen, they experience a greater steric crowding in axial compared to the equatorial position. Therefore, many substituted cyclohexane compounds prefer a conformation in which the larger substituents are in equatorial position.
