........................................................................
Answer:
The web page of a university
Explanation:
A scientist can be more biased within coming to information about pretty much anything. I have had multiple science teachers who seem more biased on to something else and pretend that they're right just cause they know what they are doing.
Then the university would be a great choice because its controlled by a higher state, then also the consistency of being updated.
It is harder to remove an electron from fluorine than from carbon because the size of the nuclear charge in fluorine is larger than that of carbon.
The energy required to remove an electron from an atom is called ionization energy.
The ionization energy largely depends on the size of the nuclear charge. The larger the size of the nuclear charge, the higher the ionization energy because it will be more difficult to remove an electron from the atom owing to increased electrostatic attraction between the nucleus and orbital electrons.
Since fluorine has a higher size of the nuclear charge than carbon. More energy is required to remove an electron from fluorine than from carbon leading to the observation that; it is harder to remove an electron from fluorine than from carbon.
Learn more: brainly.com/question/16243729
Structure of a-chloro-b-methylbutyric acid (2-chloro-3-methylbutyric acid is attached below.
The structure was drawn using following information.
1) First, the parent chain was identified. The parent chain is containing four carbon atoms, also, this chain belongs to carboxylic acid as the compound name ends with Butyric acid i.e. butyr (Butane) -ic acid (carboxylic acid).
2) Secondly, the positions of substituents were assigned by using the rule which sates that the numbering in carboxylic acid must satrt from the carbonyl carbon. Therefore, the carbon which is attached to carbonyl carbon is named as alpha (2nd position) and carbon next to alpha carbon is named as beta carbon (3rd position). Hence, we add chlorine atom on 2nd carbon next to carbonyl group and methyl group at 3rd carbon with respect to carbonyl carbon.