Answer:
33.7
Explanation:
i just know i had a question on it'
Answer:
a. 3-methylbutan-2-ol
b. 2-methylcyclohexan-1-ol
Explanation:
For this reaction, we must remember that the hydroboration is an <u>"anti-Markovnikov" reaction</u>. This means that the "OH" will be added at the <em>least substituted carbon of the double bond.</em>
In the case of <u>2-methyl-2-butene</u>, the double bond is between carbons 2 and 3. Carbon 2 has two bonds with two methyls and carbon 3 is attached to 1 carbon. Therefore <u>the "OH" will be added to carbon three</u> producing <u>3-methylbutan-2-ol</u>.
For 1-methylcyclohexene, the double bond is between carbons 1 and 2. Carbon 1 is attached to two carbons (carbons 6 and 7) and carbon 2 is attached to one carbon (carbon 3). Therefore<u> the "OH" will be added to carbon 2</u> producing <u>2-methylcyclohexan-1-ol</u>.
See figure 1
I hope it helps!
Answer:
trigonal pyramidal
Explanation:
In NF3, the nitrogen atom is sp3 hybridized. Now we must remember that according to the VSEPR theory, the number of electron pairs in the valence shell of the central atom in a molecule determines its shape.
Here, the nitrogen atom is the central atom and its outermost shell is surrounded by four electron pairs - one lone pair and three bond pairs. This means that it has a tetrahedral electron pair geometry.
However, due to the lone pair, the three fluorine atoms are arranged in a trigonal pyramidal geometry. Hence the correct shape of the molecule is trigonal pyramidal.
Widespread distribution of Permo-Carboniferous glacial sediments in South America, Africa, Madagascar, Arabia, India, Antarctica and Australia was one of the major pieces of evidence for the theory of continental drift.