A molecule that forms when atoms of the same element bond together is called a(n)________
2 answers:
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The most accurately represented John Dalton's model of the atom is: C. a tiny, solid sphere with a predictable mass for a given element
<h3>Further explanation</h3>The development of atomic theory starts from the first term conveyed by Greek scientists who suggested that every substance has the smallest particles so that the word atomos appears, which means it cannot be divided. So, John Dalton, a British scientist put forward the hypothesis about atoms, among others:
- 1. The elements are composed of atoms which are small particles which cannot be subdivided
- 2. Atoms that make up the same element have the same properties, mass, and size, while for different elements, the properties are also different
- 3. Compounds are composed of two or more atoms in a fixed ratio
- 4. In chemical reactions, atoms after and before a reaction cannot be destroyed, only separation and reassembly occur
Point 3 shows the relationship with The Law of Constant Composition of Proust so that further research on atoms is more developed
Dalton's hypothesis is described as a solid sphere like a very small shot put ball or a bowling ball based on Dalton's hobby in bowling
<h3>Learn more</h3>Bohr's model of the atom
Rutherford performed the gold foil experiment
The part of an atom that is mostly empty space
Keywords: atom, Dalton, a solid sphere, The Law of Constant Composition
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.
