Answer:
Ozone layer depletion is the thinning of the ozone layer present in the upper atmosphere. This happens when the chlorine and bromine atoms in the atmosphere come in contact with ozone and destroy the ozone molecules. One chlorine can destroy 100,000 molecules of ozone. It is destroyed more quickly than it is created
Answer:
HClO₃ /chloric acid /suffix -ic/ ClO₃⁻ (chlorate)
HClO₂/ chlorous acid/ suffix -ous/ ClO₂⁻ (chlorite)
HNO₃ /nitric acid /suffix -ic/ NO₃⁻ (nitrate)
HNO₂/ nitrous acid/ suffix -ous/ NO₂⁻ (nitrite)
Explanation:
Chlorine has 4 positive oxidation numbers to form oxyacids: +1, +3, +5 and +7.
- When it uses the oxidation number +5, it forms HClO₃, which is named chloric acid, with the suffix -ic. When it loses an H⁺, it forms the oxyanion ClO₃⁻ (chlorate).
- When it uses the oxidation number +3, it forms HClO₂, which is named chlorous acid, with the suffix -ous. When it loses an H⁺, it forms the oxyanion ClO₂⁻ (chlorite).
Nitrogen has 2 positive oxidation numbers to form oxyacids: +3 and +5.
- When it uses the oxidation number +5, it forms HNO₃, which is named nitric acid, with the suffix -ic. When it loses an H⁺, it forms the oxyanion NO₃⁻ (nitrate).
- When it uses the oxidation number +3, it forms HNO₂, which is named nitrous acid, with the suffix -ous. When it loses an H⁺, it forms the oxyanion NO₂⁻ (nitrite).
Answer:
I'm converting this if I could remember how
2.882568
2 110321/ 125000
T-T sorry if I'm wrong I have bad memory
so I recommend not using my answer at all,
if that is even how y'all write it.
c. a tertiary alcohol; when a ketone reacts with a grignard reagent followed by protonation a tertiary alcohol is formed.
More about tertiary alcohol:
No hydrogen atoms are bonded to the functional group's carbon in a tertiary alcohol. Alcohols that have a hydroxyl group bonded to the carbon atom and are linked to three alkyl groups are referred to as tertiary alcohols. These alcohols' structural makeup largely determines their physical characteristics.
This -OH group's existence enables alcohols to create hydrogen bonds with the atoms next to them. Because of this weak connection, alcohols have higher boiling points than their alkane counterparts.
The alcohol is referred to as a tertiary (3°) alcohol if the carbon atom carrying the alcohol group is connected to three other carbon atoms in the alcohol molecule.
Learn more about tertiary alcohol here:
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