Answer:
Explanation:
Let's break it down:
- Butane- A 4 carbon alkane
- Methyl - A CH₃ group
- 2,2 - Both the Methyl groups are attached at carbon 2
We can now draw the structure of 2,2-dimethyl butane using the following steps:
- Draw the backbone (butane)
- Draw the substituents (2 methyl groups at carbon 2)
Answer:
d. All of the above three answers are correct
Explanation:
Atoms are themselves built up from many smaller particles. According to Rutherford's nuclear theory (1906), the neutron and proton make up the nucleus of the atom. Atoms are electrically neutral because they contain the same number of electrons and protons. The size of atoms is about
meters. The fundamental particle of the atom is the electron.
Answer:
See the image 1
Explanation:
If you look carefully at the progress of the SN2 reaction, you will realize something very important about the outcome. The nucleophile, being an electron-rich species, must attack the electrophilic carbon from the back side relative to the location of the leaving group. Approach from the front side simply doesn't work: the leaving group - which is also an electron-rich group - blocks the way. (see image 2)
The result of this backside attack is that the stereochemical configuration at the central carbon inverts as the reaction proceeds. In a sense, the molecule is turned inside out. At the transition state, the electrophilic carbon and the three 'R' substituents all lie on the same plane. (see image 3)
What this means is that SN2 reactions whether enzyme catalyzed or not, are inherently stereoselective: when the substitution takes place at a stereocenter, we can confidently predict the stereochemical configuration of the product.