The type of charge an electron carries is B negative
Hello!
I saw this question and instantly knew I could help. I recently took a course on toxic gasses and poisons. Here's what I know.
It can be swallowed, inhaled, or absorbed through skin. It is generally released from its host compound by acids, such as the hydrochloric acid found in the stomach. The poison in the seeds is released only if the seeds are chewed.
Effects and symptoms:
Cyanide prevents the red blood cells from absorbing oxygen. It's called chemical asphyxia.
Smelling of a toxic dose of the gas can cause immediate unconsciousness, convulsions and death within one to fifteen minutes.
If swallowed a fatal dose can take up to twenty minutes or longer, esp. if swallowed on a full stomach.
If a near-lethal dose is absorbed through the skin, inhaled or swallowed the symptoms will include gasping for breath, dizziness, flushing, headache, nausea, vomiting, rapid pulse, and a drop in blood pressure causing fainting.
<span>With a lethal dose, convulsions with in four hours, except in the case of sodium nitroprusside, when death can be delayed as long as 12 hours after ingestion. </span>The victims blood may appear purple or cherry red, as in carbon monoxide poisoning, and the corpse may have pinker than normal skin.
<span>the famous bitter almond odor can be a clue and maybe noticeable at autopsy, but not everyone is capable of smelling it.
Hope this helped! :)</span>
Answer:
See explanation below
Explanation:
The question is incomplete. However in picture 1, you have the starting materials and the structure of the product, which you miss in this part.
Now, in picture 2, you have the starting reactant and the product, and the mechanism that is taking place here.
First, all what we have here is an acid base reaction. In the first step, we are using the acid medium to convert the reactant into an alcohol. The bromine there, is not leaving the molecule yet, because it's neccesary for the next step. The starting reactant is an alkene, in that way, we can convert the reactant in the first step into a secondary alcohol. In other words, the first reaction is a alkene hydration.
In the second step, we use a strong base. You may say this is a strong nucleophile and will do a Sn2 reaction to form another alcohol there, but it's not the case, because, before any kind of reaction happens, the priority here is always the acid base, so the base will react with the acidic hydrogen. In this case, it will substract an hydrogen from the OH. When this happens, the lone pair will do an auto condensation here, and attacks the bromine in the molecule. In this way, the molecule will become a cyclomolecule, and that way it form the final product.
See picture 2, for mechanism
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