
(a)
Interpretation: To determine the type of electrolyte.
Concept Introduction: An electrolyte is a substance that, when in contact with water, splits into charged ions. Positively charged ions can also be cations.
(a)

Answer to Problem 80A
Non-electrolyte
Explanation of Solution
A non-electrolyte is a solute that dissolves without dissociating, or separating, into ions. Therefore, solutions produced by the solvation of non-electrolytes will not include ions and are only made up of neutral molecules.
In the given pic, atoms of the molecules are not ionized; hence, it can be considered as a non-electrolyte.
(b)
Interpretation: To determine the type of electrolyte.
Concept Introduction: An electrolyte is a substance that, when in contact with water, splits into charged ions. Positively charged ions can also be cations.
(b)

Answer to Problem 80A
Weak-electrolyte
Explanation of Solution
A weak electrolyte is a solute that partially dissociates or separates throughout the solvation process through its component cations as well as anions.
In the given pic, it can be seen that atoms are partially ionized that’s why they can be considered weak electrolytes.
(c)
Interpretation: To determine the type of electrolyte.
Concept Introduction: An electrolyte is a substance that, when in contact with water, splits into charged ions. Positively charged ions can also be cations.
(c)

Answer to Problem 80A
Strong electrolyte
Explanation of Solution
An electrolyte that dissociates almost entirely in water is said to be a strong electrolyte. Hydrogen chloride would be a good illustration of a strong electrolyte (HCl).
In the given pic, atoms are ionized that’s why they can be considered strong electrolytes.
Chapter 15 Solutions
Chemistry 2012 Student Edition (hard Cover) Grade 11
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- Consider the molecule A,B, C and D shown below, (1 x 4) Br NH2 A OH Br 边 H B C D 1. Assign the R/S configuration to each chiral center and identify by circling all the chiral centers. 2. Draw an image for the enantiomer of each of the compounds A, B, C and D.arrow_forwardCould you crystallize one enantiomer of mandelic acid from a racemic mixture (using the typical achiral solvents found in our lab) without preparing a diastereomeric salt? Why or why not? No, because both enantiomers have the same solubility in achiral solvents. than the other. ооо Yes, because one enantiomer has a higher melting point No, because both enantiomers are liquids. Yes, because one enantiomer is more crystalline than the other.arrow_forwardIf the literature value of specific rotation for a chiral compound is -53.6°, what is the enantiomeric excess of a compound with a measured specific rotation of -40.5°?arrow_forward
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