Answer:
1) acetylide
2) enol
3) aldehydes
4) tautomers
5) alkynes
6) Hydroboration
7) Keto
8) methyl ketones
Explanation:
Acetylide anions (R-C≡C^-) is a strong nucleophile. Being a strong nucleophile, we can use it to open up an epoxide ring by SN2 mechanism. The attack of the acetylide ion occurs from the backside of the epoxide ring. It must attack at the less substituted side of the epoxide.
Oxomercuration of alkynes and hydroboration of alkynes are similar reactions in that they both yield carbonyl compounds that often exhibit keto-enol tautomerism.
The equilibrium position may lie towards the Keto form of the compound. Usually, if terminal alkynes are used, the product of the reaction is a methyl ketone.
NooooOoOOOOOɪᴏᴏɪᴡᴏᴏɪʀᴇᴡʜʜʙᴠᴇᴠᴅᴊʜʙsʙʙsʙʙᴊᴊᴊᴊʀvesebhreeje
Particles below the surface of a liquid
Answer:
photons
Explanation:
Where,
n is the number of photons
h is Plank's constant having value 
c is the speed of light having value 
is the wavelength of the light
Given that, wavelength = 514 nm = 
Energy = 10.0 mJ = 0.01 J ( 1 mJ = 0.001 J )
Applying the values as:-
photons
Answer:
Vascular plants are successful due to better transportation for water, nutrients and reproduction.
Explanation:
I got it right at school and hope this helps you learn to STUDY.jk
