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 explanation The will
solute?
A
liquids &
solution. gases 39
touch. between volatile are
correct two non-volatile two CI
correct to &
cool in of each
points similarity
0.04 the K
the of
of
the feels istemperature
fraction one of masses
containing
tempcrature.not
Is is solution Which
boiling
the
pressure
temperature.
(R) (R)
mole is atomic
LAW ReasonReason the What vapour
SOLUTION the has same
temperature. solution
if
fraction."
HENRY'S and but statement.
with
temperature, applications. °C components.
partial ofK
statement.faster? andthe 90
changes
in siatements. pressure a
atements.
change at
doubled same
for at
pressure the
mole saltion
dissolve law
-NAME (PrQ) why? its
& incorrct
corTOCtroom tle Raoult's
important volatil: solution
to
LAW statethest
bar
and vapour proportional M
CHAPTER withcorrectcorrect salt 2.5is
gas
at 5
RAOULT'liquid
S changes
is at
is (R) waterdoes at
(B)constant)
represents containing
any
respectively. "For
a
of
density
are are (R) waterofpressure gas its higher
in Reasonin conditions than of
solution(R) (R) Rcason chloride two
(Henry's directly
solution in formula ahave solution usstated the
RcasonReason but
dissolved
the
water mnention 10°C,
but waterwater law?
ofa (A). incorrect, following
ammonium waterwater when in KH will°C, is is
of and and correct,
Molality soluble following solvent X 180 a s solution
liquid forHenry'which AT
volume Assertion coldhot coldhot is gas of and Xsolute
value law and law ILaw
Gay-Lussac's
(A) (A) 'X solvent law (A)
Assertion
Assertion is is thein in in in gas 'X more solvent which and
°C Raoult's the
(A):The (A).
Assertion
of (A)(A) dissolving
salt salt
of Powdered crystals
crystals uknowa
of higherHenry'sthep°solute
K*X
p=
(b) 140 thein law
(c)law
Henry's
(a) law(b)
Raoult's Assertion
Dalton's
of
explanation
Assertion Powdered
Assertionwhich fraction is p° p law component
Assertion
(R): (A) of Identify
are ident:fy
0.08(b)0.02
(a)0.04(c) the WhichPsolute solute StateRaoult's
Both Both
Reason Salt Salt 3.An Gashave State total
B
On Under mole P p
(c) (d)
and (d) 10.
(a) (b) (C)(d) (c)
2. (a)(b) (d) 4. 5. 6. (a) 8.
7. 9.
1.
will respectively. to
fractions pure
remains
unaffected changed
(Nearest
Hg.
---mm
solution vapour of
molal
C. pressure
mole
the are 1.0 25°
the Torr,
in fractions of
their at
of B
100liquid pressure Hg vapour
molality when --mm
astemperature
mass and mole and
Torrof
Hg vapour
The fraction g/cm²
mmthe
21"C. 50
are 350ifHg is The is 1.2
mole A glucose
25°C is mmpure solution. is
-to B integer) glucose
with the and 410 of
Cooled JEENEET
at of
B thcn A
pressure solution
change becomes aqueous
(Ncarest
Hg of
ad liquids
Is A, mm solution
solution A of vapour
not liquids 50 aqucous
fraction pressure in
two Hg.
does dissociated
is aqueous
The mixingThe mm °C
solution volatíle
mole total
B. is 38 (w/v) g/mol.
g/ml. C at (w/v)
by and 38°
two0.3 is The
observcd is water 30%
x aof x
contains A 2
at
MgCI 180
is of of rcspectively.
for 30%%
respectively],
molality valuc
prcssures
MgCI, of of
is
respcctivcly pressure pressurc glucose
pressurc of of
unchange.
remain mixture
The percent
of density
Hg.l
(R):
The
Reason
with
temperaturc. solution
vapour/17 0.3 Given:vapour mm of
Vapour
mol- liquid total and0.8 mole The mass
x 24
11.The is The andinteger)aqueous The [Given:
g
35.5 thephase 0.7 80 is
water
(Molar
If 12. are0.2 13. 14.