<span>Answer:
H-C-N H-N-C C-H-N
Notice that C-H-N is the same as N-H-C just written backwards. ( i.e. they have the same connectivtiy.) You can exclude the last one with H in the middle since H has two bonds and 4 electrons around it. At this point you couldn't differentiate between the first two, so I would give you the connectivity in such a problem, which in this case is H-C-N.</span>
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.
Emulsions are an example of colloids<span> composed of tiny particles </span>suspended<span> in another immiscible (unmixable) material. An emulsion is a </span>suspension<span> of two liquids that usually do not mix together. These liquids that do not mix are said to be immiscible. An example would be </span>oil and water<span>.
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Both involve chemical bonds breaking