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.
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For the antacid analysis, the chemical reactions that occur in the titration are the following ones:
First, the antacid (composed of weak bases and carbonates) is completely neutralized by the H⁺ ions in the HCl
2HCl + CaCO₃ → CO₂ + H₂O + 2CaCl₂
HCl + OH⁻ → H₂O + Cl⁻
The titration reaction consists in titrating the excess H⁺ ions that are left in the solution, by the following reaction:
H⁺ + NaOH → H₂O + Na⁺
So, when the equivalence point is reached, the solution will go from acid to basic. As bromophenol blue is yellow in acidic solution and blue in basic solution, you'll expect the indicator to change from yellow to blue.
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A.) true
Because the rocks are formed near lava so the texture would be smooth
Fluorine - Seven electrons of it's own.
Lithium would give up one electron, so there for, fluorine is then left with eight.
The number is 25. The square root of 25 is 5 and 5x2 is 10 and then 10+5 is 15