Answer:
Acidic
Explanation:
Since the concentration of the acid is greater.
Answer:
Step 1: Identify the Individual Ions from the Reactants and Their Charges
Step 2: Switch the Cations and Anions of the reactants
Step 3: Balance the Chemical Reaction
Explanation:
i hope i helped =)
Structures of <span>
1-bromo-3-methyl-2-butene and </span>
2-bromo-3-methyl-2-butene are shown below.
It can be seen that <span>
1-bromo-3-methyl-2-butene is containing a C-H bond in which carbon is sp</span>² hybridized (i.e. =C-H) while such bonding is absent in
2-bromo-3-methyl-2-butene.
So, as we know that the peak of C-H stretching of alkenes is found in the region of 3010-3100 cm⁻¹ with medium intensity. Therefore,
1-bromo-3-methyl-2-butene will show this peak and
2-bromo-3-methyl-2-butene will lack this peak in IR spectrum.
B hoped this helps y’all g’day