Answer:
KE = 1/2*m*v^2
KE = 1/2*150kg*(20 m/s)^2
KE = 75kg * 400m²/s²
KE = 30,000 kg*m²/s²
KE = 30,000 N*m
KE = 30,000 J
Explanation:
Hope this helped.
A brainliest is always appreciated.
Answer:
The volume of air at where the pressure and temperature are 52 kPa, -5.0 ºC is
.
Explanation:
The combined gas equation is,

where,
= initial pressure of gas = 104 kPa
= final pressure of gas = 52 kPa
= initial volume of gas = 
= final volume of gas = ?
= initial temperature of gas = 
= final temperature of gas = 
Now put all the given values in the above equation, we get:


The volume of air at where the pressure and temperature are 52 kPa, -5.0 ºC is
.
Answer:
CH3OH and NADH
Explanation:
The given chemical reaction is an redox reaction in which reduction and oxidation take place.
In the process of oxidation: electrons are loss while in the process of reduction: electrons are gained.
In the given redox reaction: CH3OH + NAD --> CH2O + NADH
NAD is reduced to NADH as NADH gains one hydrogen electron while CH3OH (methanol) is oxidized to CH2O (methanal) by losing electrons.
So, CH3OH (methanol) and NADH are the reduced forms while NAD and CH2O (methanal) are oxidized forms.
Answer:
heat flow
Explanation:
heat flow moves to a higher temperature to a lower temperature
Answer:
2,2,3,3-tetrapropyloxirane
Explanation:
In this case, we have to know first the alkene that will react with the peroxyacid. So:
<u>What do we know about the unknown alkene? </u>
We know the product of the ozonolysis reaction (see figure 1). This reaction is an <u>oxidative rupture reaction</u>. Therefore, the double bond will be broken and we have to replace the carbons on each side of the double bond by oxygens. If
is the only product we will have a symmetric molecule in this case 4,5-dipropyloct-4-ene.
<u>What is the product with the peroxyacid?</u>
This compound in the presence of alkenes will produce <u>peroxides.</u> Therefore we have to put a peroxide group in the carbons where the double bond was placed. So, we will have as product <u>2,2,3,3-tetrapropyloxirane.</u> (see figure 2)