1) <u>Stereo-selective (or enantioselective)</u> reactions form predominately or exclusively one enantiomer.
2) Epoxidation is the addition of a single oxygen atom to an alkene to form an epoxide.
3) <u>Hydrogenation (or reduction)</u> of an alkene forms an alkane by addition of H₂.
4) <u>Dihydroxylation</u> is the addition of two hydroxy groups to a double forming, a 1,2-diol or glycol.
5) <u>oxidative</u> cleavage of an alkene breaks both the σ and π bonds of the double bond to form two carbonyl groups.
6) <u>Regioselective</u> reactions form predominately or exclusively one constitutional isomer.
7) <u>Syn</u> dihydroxylation results when an alkene is treated KMnO4 or OsO4, where each reagent adds two oxygen atoms to the same side of the double bond.
Answer:
An egg will be your ans because it needs to be broken before we can cook it or use it for making other delicases
Explanation:
<em><u>Hope </u></em><em><u>it </u></em><em><u>helps </u></em>
Answer:
The yeast present contains an enzyme called catalase which catalyses the reaction. More the amount of the catalyst added, faster will be the decomposition of the hydrogen peroxide.
Answer:
Explanation:
H ₂ S O ₄ + 2 N a O H ⟶ 2 H ₂ O + N a ₂ S O ₄
29.09 mL of 0.639 M N a O H is mixed with 213.8 mL of H ₂ S O ₄
Let the concentration of H ₂ S O ₄ be S₂ .
In terms of normal or equivalent solution is will be 2 N solution
From the formula S₁ V₁ = S₂ V₂
= 29.09 x .639 = 213.8 x S₂
S₂ = .087 N solution
In terms of molar solution it will be .087 / 2 M
= .0435 M
