Answer:
Q14: 17,140 g = 17.14 kg.
Q16: 504 J.
Explanation:
<u><em>Q14:</em></u>
- To solve this problem, we can use the relation:
<em>Q = m.c.ΔT,</em>
where, Q is the amount of heat absorbed by ice (Q = 3600 x 10³ J).
m is the mass of the ice (m = ??? g).
c is the specific heat of the ice (c of ice = 2.1 J/g.°C).
ΔT is the difference between the initial and final temperature (ΔT = final T - initial T = 100.0°C - 0.0°C = 100.0°C).
∵ Q = m.c.ΔT
∴ (3600 x 10³ J) = m.(2.1 J/g.°C).(100.0°C)
∴ m = (3600 x 10³ J)/(2.1 J/g.°C).(100.0°C) = 17,140 g = 17.14 kg.
<u><em>Q16:</em></u>
- To solve this problem, we can use the relation:
<em>Q = m.c.ΔT,</em>
where, Q is the amount of heat absorbed by ice (Q = ??? J).
m is the mass of the ice (m = 12.0 g).
c is the specific heat of the ice (c of ice = 2.1 J/g.°C).
ΔT is the difference between the initial and final temperature (ΔT = final T - initial T = 0.0°C - (-20.0°C) = 20.0°C).
∴ Q = m.c.ΔT = (12.0 g)(2.1 J/g.°C)(20.0°C) = 504 J.
The heat required to vaporize 43.9 g of acetone at its boiling point is calculated as below
the heat of vaporization of acetone at its boiling point is 29.1 kj/mole
find the moles of acetone = mass/molar mass
= 43.9g /58 g/mol =0.757 moles
heat (Q) = moles x heat of vaporization
= 29.1 kj/mole x 0.757 moles = 22.03 kj
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.