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: try to understand coz the question is not valid
Explanation: Explain the relationship between forward and reverse reactions at equilibrium and predict how changing the amount of a reactant or product (creating a stress) will affect that relationship.For example (select one from each underlined section)If the amount of (reactant or product) increases, the rate of the (forward or reverse)reaction will (increase or decrease)to reach a new equilibrium. If the amount of (reactant or product) decreases, the rate of the (forward or reverse)reaction will (increase or decrease)to reach a new equilibrium. Procedure: Access the virtual lab and complete the inquiry experiment
<span>35.0 mL of 0.210 M
KOH
molarity = moles/volume
find moles of OH
do the same thing for: 50.0 mL of 0.210 M HClO(aq) but for H+
they will cancel out: H+ + OH- -> H2O
but you'll have some left over,
pH=-log[H+]
pOH
=-log[OH-]
pH+pOH
=14</span>
Answer:
1230
Explanation:
1.20×1025=1230 is your answer
Answer:
if i got it right i think it woud be a
