Answer:
O D. It has an -OH group attached to the end of the molecule.
Explanation:
Some alcohols have hydroxyl group (OH) attached to the end of a molecule and some have it attached as a branch on the molecule

- R is aryl or alkyl group
- OH is hydroxyl group
Answer:
Option-B (2-methylpropene)
Explanation:
The reaction scheme is attached below,
In first step the alkene acts a nucleophile and adds H⁺ across double bond yielding a stable tertiary carbocation.
In the second step the oxygen atom of methanol acts as nucleophile and attacks the positive charge carrying carbon atom resulting in the formation of t-butyl methyl ether.
Answer:
By transfer of electron from electropositive to electronegative elements
Explanation:
Examples are NaCl, MgO, Al2O3
Ca(OH)₂ ==> Ca²⁺ + 2 OH<span>-
Ca(OH)</span>₂ is <span>strong Bases</span><span>
</span>Therefore, the [OH-] equals 5 x 10⁻⁴ M. For every Ca(OH)₂ you produce 2 OH⁻<span>.
</span>
pOH = - log[ OH⁻]
pOH = - log [ <span>5 x 10⁻⁴ ]
pOH = 3.30
pH + pOH = 14
pH + 3.30 = 14
pH = 14 - 3.30
pH = 10.7
hope this helps!</span>