5. is b
but im not sure about 4
hope this helps
Specialized proteins which function as catalysts for organic reactions are enzymes.
C. Fewer habitats for wild animals to live in
Explanation:
Biodiversity does not directly impact humans in that there are fewer habitats for wild animals to live in. This is a direct impact on animals and not humans.
Biodiversity is the variation of life forms in an area. It is measured by the ability of the ecosystem to sustain different life forms and keep their interaction with the environment.
It helps to maintain and sustain life.
To humans, reducing biodiversity;
- reduces the potential of medicine derived from other organisms. When their habitat is lost, we lose them.
- fewer ecosystems to appreciate for beauty and recreation. It leads to loss of the ecosystem.
- fewer wild food species for humans to eat.
Loss of habitat directly affects wild animals and not man.
learn more:
Biodiversity hotspots brainly.com/question/10723602
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Answer:
How the incident happened
Any chemicals involved in an incident
Any other hazards present in the lab
Explanation:
Above are the types of information that are necessary to communicate with emergency responders. The emergency responders ask the first question that how the incident happened. After that they ask that is there any harmful chemicals are present in the laboratory or what types of chemicals present in the laboratory. These questions were asked by the emergency responders in order to give the patient a suitable treatment.
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.