Cl-35, as the atomic mass of Chlorine (35.45) is closer to the number 35 than to the number 37. A higher abundance of CL-35 isotope would have caused the atomic number (which is an average of the values of all isotopes of a substances taking relative abundance into consideration) to decrease from 36, which would appear to be the average.
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!
The options for given question are as follow,
1) Methane molecules show hydrogen bonding.
<span>2) Ammonia molecules show hydrogen bonding. </span>
<span>3) Methane has stronger hydrogen bonding than ammonia. </span>
<span>4) Both the compounds do not show hydrogen bonding. </span>
<span>5) Both the compounds have strong hydrogen bonding.
</span>
Answer:
Correct answer is Option-2 (Ammonia molecules show hydrogen bonding).
Explanation:
Hydrogen bond interactions are formed when a partial positive hydrogen atom attached to most electronegative atom of one molecule interacts with the partial negative most electronegative element of another molecule. So, in Ammonia hydrogen gets partial positive charge as nitrogen is highly electronegative. While the C-H bond in Methane is non-polar and fails to form hydrogen bond interactions.
<span>283.89 g/mol is the molar mass of tetraphosphorus decoxide</span>
