Answer:
180º
Explanation:
Carbon has 4 valence electrons and to complete the octet requires 4 more , so it will share with the oxigen atoms 4 more, forming a single and a pi bond similar to CO2
Since the carbon does not have lone pairs, the geometry around this central atom will be linear and the angle will be 180 , S = C = S
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.
The best answer is the isotope of strontium which is strontium-85. It has a half-life of about 64 days. The metal strontioum has four stable, naturally occurring isotopes which includes 84Sr (0.56%), 86Sr (9.86%), 87Sr (7.0%) and 88Sr (82.58%).