Answer: assume pathogens are present and treat the samples accordingly
Explanation:
When investigators are unable to conclusively ascertain the source of a biological sample found at a crime scene, the correct thing to do is to treat it as if pathogens are present in it and handle it according to set rules on how to handle pathogens.
This is done to ensure that if a pathogen is indeed present, it would not cause a health emergency by infecting those who come in contact with the samples at the scene.
Answer:
If you see in the image above, there is an unbalance force applied while playing tug of war. Since it is 1 vs 2, there is a greater net force in the right side then the left side. If it was 2 vs 2 or 1 vs 1, then they are appling balance force. You can also see in the picture that the arrows are pointing outwards (--->) rather then inwards (<---) because you are pulling the rope not pushing the rope. If you add one person on the left side, then the newtons which is 20N will become to 35N and will be balanced, but since there in only 1 person, there is less force on the left side, the newtons gets subtracted having only 20N. Since you are pulling the rope, the friction is opposite (<---). Since you are pulling the rope, you are using Kinetic force and the rope stays in potential force since it stays constant.
Hope this helps, thank you :) and I am not sure about magnitude I think you can that since there is greater force on the right side, there is more magnitude there.
Answer:
See explanation and picture below
Explanation:
First, in the case of methyloxirane (Also known as propilene oxide) the mechanism that is taking place there is something similar to a Sn2 mechanism. Although a Sn2 mechanism is a bimolecular substitution taking place in only step, the mechanism followed here is pretty similar after the first step.
In both cases, the H atom of the HBr goes to the oxygen in the molecule. You'll have a OH⁺ in both. However, in the case of methyloxirane the next step is a Sn2 mechanism step, the bromide ion will go to the less substitued carbon, because the methyl group is exerting a steric hindrance. Not a big one but it has a little effect there, that's why the bromide will rather go to the carbon with more hydrogens. and the final product is formed.
In the case of phenyloxirane, once the OH⁺ is formed, the next step is a Sn1 mechanism. In this case, the bond C - OH⁺ is opened on the side of the phenyl to stabilize the OH. This is because that carbon is more stable than the carbon with no phenyl. (A 3° carbon is more stable than a 2° carbon). Therefore, when this bond opens, the bromide will go there in the next step, and the final product is formed. See picture below for mechanism and products.
Explanation:
option A skeleton system is correct option
hope this helps you !
