Answer:
Ethanol has covalent intramolecular bonds. Ethanol is polar. Ethanol has dispersion intermolecular forces. Dimethyl ether is polar. Dimethyl ether forms hydrogen bonds. Dimethyl ether has dispersion intermolecular forces.
Explanation:
Ethanol is not a carboxylic acid. It is an alcohol and it has covelent intramolecular bonds. It is polar and it also has dispersion intermolecular forces.
Dimethyl ether is also polar and it has forms hydrogen bonds. It also has dispersion intermolecular forces. Dimethyl ether does not have ionic intramolecular forces
The black fur absorbs all the colors where the white fun reflects all the colors because we see the green grass it absorbs all the colors except green and the yellow dandelion is reflecting yellow and orange because it’s color is like a mix of them but it still absorbs the other colors
Melting, vaporization, boiling, and sublimation.
<span>If I done the math correctly it is 3729J because you multiply 16.5 g by the 2260 J/g and get 3729 J</span>
Answer:
Reagents: 1) 
2) 
, 
Mechanism: Hydroboration
Explanation:
In this case, we have a <u>hydration of alkene</u>s reaction. But, in this example, we have an <u>anti-Markovnikov reaction</u>. In other words, the "OH" is added in the least substituted carbon. Therefore we have to choose an anti-Markovnikov reaction: <u>"hydroboration"</u>.
The <u>first step</u> of this reaction is the addition of borane () to the double bond. Then in the <u>second step</u>, we have the deprotonation of the hydrogen peroxide, to obtain the peroxide anion. In the <u>third step</u>, the peroxide anion attacks the molecule produced in the first step to produce a complex compound in which we have a bond "
". In <u>step number 4</u> we have the migration of the C-B bond to oxygen. Then in <u>step number 5</u>, we have the attack of on the 
to produce an alkoxide. Finally, the water molecule produce in step 2 will <u>protonate</u> the molecule to produce the alcohol.
See figure 1
I hope it helps!
