Answer:
No, it's a physical reaction.
Explanation:
A chemical change produces new chemical compounds, but combining water and powder is just mixing the powder with the water. It's not a new compound.
I don't know how to really explain, sorry :)
Answer:
M = 16.8 M
Explanation:
<u>Data:</u> HNO3
moles = 12.6 moles
solution volume = 0.75 L
Molarity is represented by the letter M and is defined as the amount of solute expressed in moles per liter of solution.

The data is replaced in the given equation:

The balanced reaction
is:
4NH3 + 3O2 --> 2N2 + 6H2O
<span>We
are given the amount of reactants to be used for the reaction. This
will be the starting point of our calculation.</span>
83.7g of O2 ( 1 mol / 32 g) = 2.62 mol O2
2.81 moles of NH3
From the balanced reaction, we have a 4:3 ratio of the reactants. The limiting reactant would be oxygen. We will use the amount for oxygen for further calculations.
<span>2.62 mol O2</span><span> (6 mol H2O / 3 mol O2) (18.02 g H2O / 1 mol H2O) = 94.42 g H2O</span>
Answer : The correct answer for a) 4-bromo-2-iodo-4-methyl pentane and b)5-bromo-2-ethoxy-2-methyl pentane.
A) Reaction with NaI :
Reaction of alkyl halide with NaI is known as Finkelstein Reaction . The acetone is used as solvent . It involves bimolecular nucleophillic substitution rmechanism (SN²) . There is replecement of one halogen with other occurs .
The incoming Nucleophile(Nu⁻) (halide) attacks on carbon from back side , while the leaving group (halide) leaves the compound from front side , simultaneously. The product so formed have is inverted .(Image)
NaI releases I⁻ ion which act as nucelophile and attacks on C1 carbon and Br⁻ from C1 carbon is released . Out of two bromines at C1 and C4 carbons , C1 is primary carbon which is less sterically hindered while C-4 is tertiary carbon and sterically hindered . So it is easy for incoming Nu⁻ to attack on C1 carbon .So Br⁻ is repleaced by I⁻.
1,4-dibromo-4-methylpentane + NaI → 4-bromo-1-iodo-4-methylpentane
The product formed from reaction between 1,4-dibromo-4-methylpentane and NaI is 4-bromo-1-iodo-4-methylpentane . (Image)
B) Reaction with AgNO3 :
Reaction of alkyl halide with AgNO3 in ethanol takes place via SN¹ ( unimolecular nucleophilic substitution ) mechanism . In this leaving group(halide) leaves from alkyl halide forming an intermediate carbocation species . The incoming Nu⁻ attack on this carbocation.
AgNO3 reacts releases Ag⁺ion which abstract Br⁻ of C-4 carbon from 1,4-dibromo-4-methylpentane. THis forms tertiary carbocation which is more stable than carbocation formed by removal of Br from C-1 . The ethanol being more Nucleophilic than NO₃⁻ (from AgNO₃), attacks on this carbocation .(Image )
The product formed as a result is 5-bromo-2-ethoxy-2-methyl pentane.