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.
Answer:
33.3 g AlCl3
Explanation:
First:
You need a balanced chem equation.
2Al + 3Cl2 --->2AlCl3
So now you use this to set up train track method which helps us cancel out the units. Also we dont care about chlorine because it is excess.
6.73g Al x 1mol Al/26.98g Al x 2mol AlCl3/2molAl x 133.34g AlCl3/1molAlCl3
= 33.3 g AlCl3
C and A because the product of a matter will always be the same and just google A.
Glaciers cause erosion in two main ways: plucking and abrasion. Plucking is caused when sediments are picked up by a glacier. They freeze to the bottom of the glacier and are carried away by the flowing ice. ... The rocks and sediment grind away as the glacier moves
