Answer:
Acetylide , Enol ,aldehydes, tautomers, alkynes , Hydroboration, Keto
Explanation:
Reset <u>Acetylide</u> anions are strong nucleophiles that open epoxide rings by an SN2 mechanism. <u>Enol </u>tautomers have an O-H group bonded to a C=C. <u>aldehydes </u>are formed from terminal alkynes with the addition of water using BH3 then H2O2. <u>tautomers</u> are constitutional isomers that differ in the location of a double bond and a hydrogen and exist in an equilibrium with each other. <u>alkynes</u> are compounds that contain a carbon-carbon triple bond. <u>Hydroboration</u> of a terminal alkyne adds BH₂ to the less substituted, terminal carbon.<u> Keto</u> tautomers have a C=O and an additional C-H bond.
Answer:
There is an extra O2 molecule left over
Explanation:
Sugar. It is solid and its atoms have less kinetic energy to overcome the bonding force. So, the bonding force is stronger than water, which is liquid and has more kinetic energy to overcome the bonding force of atoms. So, water has less strong force of attraction. Hence, sugar has stronger forces of attraction.
Answer:
ok
Explanation:
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