Answer:
Option A.
2Na + 2H2O —> 2NaOH + H2
Explanation:
To know which option is correct, we shall do a head count of the number of atoms present on both side to see which of them is balanced. This is illustrated below below:
For Option A:
2Na + 2H2O —> 2NaOH + H2
Reactant >>>>>>> Product
2 Na >>>>>>>>>>> 2 Na
4 H >>>>>>>>>>>> 4 H
2 O >>>>>>>>>>>> 2 O
Thus, the above equation is balanced.
For Option B:
2Na + 2H2O —> NaOH + H2
Reactant >>>>>>> Product
2 Na >>>>>>>>>>> 1 Na
4 H >>>>>>>>>>>> 3 H
2 O >>>>>>>>>>>> 1 O
Thus, the above equation is not balanced.
For Option C:
2Na + H2O —> 2NaOH + H2
Reactant >>>>>>> Product
2 Na >>>>>>>>>>> 2 Na
2 H >>>>>>>>>>>> 4 H
1 O >>>>>>>>>>>> 2 O
Thus, the above equation is not balanced.
For Option D:
Na + 2H2O —> NaOH + 2H2
Reactant >>>>>>> Product
1 Na >>>>>>>>>>> 1 Na
4 H >>>>>>>>>>>> 5 H
2 O >>>>>>>>>>>> 1 O
Thus, the above equation is not balanced.
From the illustrations made above, only option A is balanced.
Answer:
0.36 m/s
Explanation:
im in 8th grade in honors science and i think, since u have distance and time you have to divide distance by time
<h3><u>Full Question:</u></h3>
The following compound has been found effective in treating pain and inflammation (J. Med. Chem. 2007, 4222). Which sequence correctly ranks each carbonyl group in order of increasing reactivity toward nucleophilic addition?
A) 1 < 2 < 3
B) 2 < 3 < 1
C) 3 < 1 < 2
D) 1 < 3 < 2
<h3><u>Answer: </u></h3>
The rate of nucleophilic attack of carbonyl compounds is 2<3 <1.
Option B
<h3><u>Explanation. </u></h3>
Nucleophilic attack is explained as the attack of an electron rich radical to a carbonyl compound like aldehyde or a ketone. A nucleophile has a high electron density, so it searches for a electropositive atom where it can donate a portion of its electron density and become stable.
A carbonyl compound is a 
hybridized carbon atom with a double bonded oxygen atom in it. The oxygen atom pulls a huge portion of electron density from carbon being very electropositive.
In a ketone, there are two factors that make it less likely to undergo a nucleophilic attack than aldehyde. Firstly, the steric hindrance of two carbon groups being attached with the carbonyl carbon makes it harder for the nucleophile to approach. Secondly, the electron push by the carbon groups attached makes the carbonyl carbon a bit less electropositive than the aldehyde one. So aldehydes are more reactive towards a nucleophilic addition reaction.
Answer:Noble gases:
are highly reactive.
react only with other gases.
do not appear in the periodic table.
are not very reactive with other elements.
Explanation:Noble gases:
are highly reactive.
react only with other gases.
do not appear in the periodic table.
are not very reactive with other elements.
1.curium ( 1944 Marie and Pierre Curie
<span>2.einsteinium ( Albert Einstein) </span>
<span>3.fermium (1953 Enrico Fermi) </span>
<span>4.mendelevium (1955 Dmitri Mendeleev, who devised first Periodic Table) </span>
<span>5.nobelium ( 1957 Alfred Nobel) </span>
<span>6.niobium (1801 Niobe/ daughter of Tantalus) </span>
<span>7.samarium (1879 Samarski, a Russian engineer) </span>
<span>8.titanium (1791 Greek mythology, Titans, first sons of earth) </span>
<span>9.thorium ( 1819 named after Thor of course !!!:) ) </span>
<span>10.tantalum ( 1802 Tantalus of Greek mythology) pick which ever best that your more into hope this helped you alot:/</span>
