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.
Formation of ammonia by nitrogen and hydrogen is habers process wher 28g N2 results in formation of 34g NH3
so 35g N2 will form 34*35/28=42.5g NH3 where it given that reaction takes place in excess of H2
N2+3H2 gives 2NH3
Answer:
The answer is C
Explanation:
This is the answer because it is the only way that it is okay to split in half.
Answer : A and D shows PROCESS of sweating