Answer:
cis 2,3-dibromo- 2-butene
trans 2,3-dibromo- 2-butene
Explanation:
The cis-trans or geometric isomerism is due to restricted rotation around a carbon-carbon bond. This restriction may be due to the presence of double bonds or cycles.
The carbon-carbon double bond prevents free rotation of atoms in molecules. These two molecules have the same atoms, but they are different molecules. They are geometric isomers to each other.
The given compound can exist in the form of two isomers, cis and trans. The isomer that has the substituents on the same side is called cis, and the one that has them on opposite sides is trans.
Hello!
You would expect to observe
2 triplets in the ¹H NMR spectra for o-chlorotoluene.
Multiplicity observed in ¹H NMR spectra when the atom couples with a neighbor ¹H atom. The multiplicity is equal to
N+1 where N is the number of neighbor atoms.
To observe a triplet, you'll need a molecule with 2 neighbor atoms. In o-chlorotoluene (shown in the figure), only protons C and D have 2 neighbor atoms (B and D; A and C, respectively), so you'll expect to see a 2 triplets.
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The valence electrons determine how reactive an element is, and since Sodium and other alkali metals could easily lose an electron, they become very reactive to be stable.
Answer: 350torr
Explanation: it will reach such i high pressure level that it will reach contobey level
