Carbonation isn’t a force that causes such
Answer:
5-chloro-2-methylcyclohexanol
Explanation:
There is no structure for the compound, but we can analyze the proposed options using the IUPAC rules to name organic compounds.
IUPAC rules state that to name an organic compound, first we have to identify the priorities for the functional groups present in the compound. <em><u>In this case, the priority functional group is the alcohol group</u></em>, <u><em>so we will start the counting of the carbons in this group.</em></u> Then, the counting of carbon atoms is followed by the next substituents so they have the lowest possible numbers, <em><u>in this case, we can assign the number 2 to the methyl group and 5 to the chloride group</u></em>, and name the compound in alphabetical order, using commas to separate the words from the numbers and with no space between the words.
Since the other options involve: <u>high countings for the susbtituents groups (</u><u>3</u><u>-chloro-</u><u>6</u><u>-methylcyclohexanol)</u>, <u>wrong assignation of priority functional group (</u><u>1-chloro</u><u>-4-methylcyclohexanol), wrong sequence of counting in the compound (</u><u>2-methyl-3-chloro</u><u>cyclohexanol) and no alphabetical order to name the compound (2-</u><u>methyl</u><u>-5-</u><u>chloro</u><u>cyclohexanol), </u><u>the correct option is:</u>
5-chloro-2-methylcyclohexanol
Have a nice day!
Answer is (1) - N
<em>Explanation:</em>
I think the given chart is electronegativity chart.
Electronegativity is a
value that tells us how an atom can attract electrons towards itself. <span><u>If the electronegativity is
high, then the attraction to the electrons is high unless the attraction to the
electrons is low. </u>
Electronegativity increases from left to right of the periodic table and decreases from up to down.
Hence, highest electronegative atom is F which has 4.0 and lowest electronegative atoms are Cs and Fr (0.7).
The electronegativity values for given atoms are
N - 3.0
Na - 0.9
P - 2.1
Pt - 2.2
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