Answer:
The reaction would take place with racemization.
Explanation:
The compound (R)-3-bromo 3-methylhexane contains has the leaving group attached to a tertiary carbon atom. When the leaving group is attached to a tertiary carbon atom, the compound undergoes nucleophilic substitution via SN1 mechanism. This mechanism involves the formation of a planar carbocation intermediate. The nucleophile may attack this intermediate from either faces, leading to racemization of the product.
B. position.
Potential energy is associated with position.
Explanation:
When carbon atom tends to form single bonds then its hybridization is
, when carbon atom tends to form double bond then its hybridization is
and when a carbon atom is attached to a triple bond or with two double bonds then its hydridization is sp.
For example, in HCN molecule there is a triple existing between the carbon and nitrogen atom.
So, hybridization of carbon in this molecules is sp. Moreover, nitrogen atom is also attached via triple bond and it also has a lone pair of electrons. Hence, the hybridization of nitrogen atom is also sp.
Thus, we can conclude that s and p type of orbitals overlap to form the sigma bond between C and N in H−C≡N:
Answer: The weight/weight % or percent by mass of the solute is 5.41 %.
Explanation:
Mass of the sodium sulfate,w = 9.74 g
Volume of the water = 165 mL
Density of the water = 1 g/mL

Mass of the water =
Mass of the solution, W:
Mass of solute + Mass of solvent =9.47 g + 165 g=174.47 g

The weight/weight % or percent by mass of the solute is 5.41 %.