When 2-methyl-3-hexene is treated with Cl2 in methanol, three products are formed (neglecting stereoisomers). Draw curved arrows
1 answer:
Answer:
Explanation:
The structural formula of 2-methyl-3-hexene is drawn in the attached image below. After then, the three possible structures were drawn and the mechanism reaction.
From the mechanism shown, methanol deprotonates methoxide proton and neutralizes the positive charge to form methoxide. This is followed by the movement of electrons that takes place from the region of higher electron density to lower electron density.
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Answer:
1 and 2
Trigonal planar
Tetrahedral
Trigonal Planar
Linear
Bent ( v- shape)
Explanation:
The highlighted atoms has a delocalized lone pair - 1 and 2
All sp2-hybridized carbon atoms have geometry- Trigonal planar
All sp3-hybridized carbon atoms have geometry - Tetrahedral
The nitrogen atom has geometry - Trigonal Planar
The oxygen atom of the C=O bond has geometry - Linear
and the other oxygen atom has geometry - Bent ( v- shape)
P.S - The correct question is -
Answer:
Explanation:
According to the law of conservation of mass, mass can neither be created nor be destroyed. Thus the mass of products must be same as the mass of reactants.
For the conservation of mass, the number of atoms of each element must be same in reactants and products. Thus we need to balance the reaction by writing appropriate stochiometric coefficients.
All the hydrocarbons burn in oxygen to form carbon dioxide and water.Thus the complete balanced equation is: