Answer:
Butan-2-one
Explanation:
1. 1700 cm⁻¹
A strong peak near 1700 cm⁻¹ is almost certainly a carbonyl (C=O) group.
2. Triplet-quartet
A triplet-quartet pattern indicates an ethyl group.
The 2H quartet is a CH₂ adjacent to a CH₃. The peak normally occurs at δ 1.3, but it is shifted 1.2 ppm downfield to δ 2.47 by an adjacent C=O group.
The 3H triplet at δ 1.05 is the methyl group. It, too, is shifted downfield from its normal position at δ 0.9. The effect is smaller, because the methyl group is further from the carbonyl.
3. 3H(s) at δ 2.13
This indicates a CH₃ group with no adjacent hydrogen atoms.
It is shifted 0.8 ppm downfield to δ 2.13 by the adjacent C=O group.
4. Identification
The identified pieces are CH₃CH₂-, -(CO)-, and -CH₃. There is only one way to put them together: CH₃CH₂-(C=O)-CH₃.
The compound is butan-2-one.
45 is the atomic mass of the atom. And the name is Scandium
I believe it’s because they are trying to find other things that won’t pollute the environment as much, and they are also doing this because we are trying to reduce green house gas. Sorry if i’m wrong :(
Answer:
The third one makes the most sense
Explanation:
Dehydrohalogenation reactions occurs as elimination reactions through the following mechanism:
Step 1: A strong base(usually KOH) removes a slightly acidic hydrogen proton from the alkyl halide.
Step 2: The electrons from the broken hydrogen‐carbon bond are attracted toward the slightly positive carbon (carbocation) atom attached to the chlorine atom. As these electrons approach the second carbon, the halogen atom breaks free.
However, elimination will be slower in the exit of Hydrogen atom at the C2 and C3 because of the steric hindrance by the methyl group.
Elimination of the hydrogen from the methyl group is easier.
Thus, the major product will A
