Professional Documents
Culture Documents
9 April 2019 Shift 1
9 April 2019 Shift 1
Solutions
PHYSICS
1. (d) Given, kinetic energy = kq2 Substituting these given values in Eq. (i),
we get
We know that, kinetic energy of a rotating body
1 500
about its axis = Iw2 \ vrms, 2 = ´ 200 m/s
2 400
where, I is moment of inertia and w is angular 1
= 5 ´ 200 m/s = 100 5 m/s
velocity. 2
1 2 2kq2 3. (a) Let the length of each side of square ABCD
So, Iw = kq2 or w2 =
2 I is a.
2k R
Þ w= q … (i) \Resistance per unit length of each side =
I 4a
A B
Differentiating the above equation w.r.t. time
on both sides, we get R2
dw 2k dq 2k é dq ù
= × = ×w êQw =
dt I dt I ë dt úû
\ Angular acceleration,
dw 2k 2k 2k
a= = ×w= × q [using Eq. (i)]
dt I I I
2k
or a = q D R1 C
I E
Alternate Solution R R a R
Now, R1 =[EC ] = ´ =
2kq2 4a 4a 2 8
As, w2 =
I R R 7a 7R
dw 2k dq Similarly, R2 = [EDABC ] = ´ =
Þ 2w = × 2q 4a 4a 2 8
dt I dt Now, effective resistance between E and C is
2k the equivalent resistance of R1 and R2 that are
or w dw = q dq
I connected in parallel as shown below.
dw 2k
w (= a ) = ×q R1
dq I
2k
or a= q E
I C
\Taking the ratio of h1 , h2 and h3 by using So, when radius is doubled, height becomes half.
Eqs. (i), (ii) and (iii), we get \ h¢ = h / 2
v2 3 v02 7 v02 mass(M )
h1 : h2 : h3 = 0 : : Now, density (r) =
g 4 g 10 g volume(V )
3 7 Þ M = r ´ pr 2h
= 1: :
4 10 \ M ¢ = rpr ¢2 h ¢
Þ h1 : h2 : h3 = 40 : 30 : 28 = 20 : 15 : 14 M ¢ r ¢2 h ¢ (2r )2 (h / 2)
\ = 2 = =2
\ The most appropriate option is (c). M r h r 2h
Although, it is still not in the correct sequence. Þ M ¢ = 2M
Alternate Solution Alternate Solution
Total kinetic energy of a rolling body is also According to the given figure, force inside the
given as capillary tube is
1 é K2ù
Etotal = mv2 ê1 + 2 ú 2prT
2 ë R û
where, K is the radius of gyration.
Using conservation law of energy,
1 é K2ù Mg
mv2 ê1 + 2 ú = mgh
2 ë R û 2prT = Mg Þ M µ r
v2 é K2ù When r ¢ = 2r, then
or h= ê1 + 2 ú
2g ë R û M ¢ = 2M
Q = CV = 10 ´ 10-6 ´ 20
6W
Þ Q = 2 ´ 10-4 C = 200 mC
18. (d) (L – L /n)
72V 4W 12W
4 ´ 12
In parallel, Req = = 3W L /n
4 + 12
Þ
I 6W
In series, Req = 6W + 3W = 9W
…(i) L /n
9W
Now, centre of mass of the hanged part
will be its middle point.
72V So, its distance from the top of the
table will be L / 2n.
\Initial potential energy of the hanged
V 72 part of cable,
So, current in steady state, I = = = 8A
R 9 æMö æ L ö
Ui = ç ÷ (- g ) ç ÷
Now, by using current division, at point P, èn ø è 2n ø
current in 6 W branch is MgL
Þ Ui = - …(ii)
72 - VP 2n 2
= 8A
6W When whole cable is on the table,
Þ VP = 72 - 48 = 24 V its potential energy will be zero.
\ Uf = 0 …(iii)
APRIL ATTEMPT ~ 09 April 2019, Shift I 7
CHEMISTRY
1 (c) Aromatic electrophilic substitution Given reaction is,
reactions are fast in those compounds in which Zn + Cu 2+ ¾® Zn 2+ + Cu
the attacking site possess high electron
density. Electron withdrawing groups (EWGs) Eº cell = 2.0 V
reduces the electron density in the benzene F = 96000 C
ring due to its strong –I effect and makes
n=2
further substitution difficult. Hence, called as
deactivating groups. While electron releasing To find the value of DGº (kJ mol), we use the
groups (ERGs) increases the electron density in formula
the benzene due to resonance. Therefore, DG º = - nFE º cell
activates the benzene ring for the attack by an
electrophile. Hence, called as activating groups. DGº = -2 ´ 96000 ´ 2
In given options, = -384000 J/mol
·· -384000
Activating groups are — CH3 < — O CH3 In terms of kJ/mol, DGº =
·· 1000
( +I , +R ) Strong +R effect
= -384 kJ/mol
Deactivating groups are — CN > — Cl
Strong – I effect ( -I > -R )
3 (c) Key Idea PBr3 reagent is used for the substitution
So, the correct order is of —Br group while alc. KOH reagent is used to
CN Cl Me OCH3 carry out elimination reaction.
Step II 3-bromohexanone in presence of Here, H2 gas does not act as limiting reagent
alc. KOH undergoes elimination reaction and since 7.5 g of H2 gas is required for 35g of N2
gives cyclohex-2-en-1-one. and 8g of H2 is present in reaction mixture.
Mass of H2 left unreacted = 8 - 7.5 g of H2.
Alc. KOH
Br = 0.5 g of H2.
Similarly, in option (c) and (d), H2 does not act
O O as limiting reagent.
Cyclohex-2-en-1-one For 14g of N2 + 4 g of H2.
4 (b) Statement-(b) is not true for sucrose. It is As we know 28g of N2 reacts with 6g of H2.
6
linked through a glycosidic linkage between 14g of N2 reacts with ´ 14 g of H2 Þ 3g of H2.
C-1 of a-glucose and C-2 of b-fructose. Since, 28
the reducing groups of glucose and fructose are For 28g of N2 + 6 g of H2, i.e. 28g of N2 reacts
involved in glycosidic bond formation, sucrose with 6g of H2 (by equation I).
is a non-reducing sugar.
6 (b) In presence of alc. KOH, the given halide
CH2OH undergoes elimination reaction.
O
H H HOH2C O Alc. KOH
H H
a b Cl
OH H Cl Cl
HO Glycosidic
linkage H HO CH2OH
H OH The alkene produced undergoes polymerisation
via free radical mechanism. This process
a-D-glucose OH H involve three steps, i.e. initiation, propagation
b-D-fructose and termination.
On hydrolysis with acids or enzyme, sucrose
gives equimolar mixture of D-(+)-glucose and Polymerisation n
D-(–)-fructose.
HCl
C12H22O11 + H2O ¾¾® C6H12O 6 + C6H12O 6 Cl Cl
D-(+) -glucose D-(–)-fructose Polymer
5 (a) Key Idea The reactant which is present in the 7 (d) q (heat) and W (work) represents path
lesser amount, i.e. which limits the amount of functions. These variables are path dependent
product formed is called limiting reagent. and their values depends upon the path
followed by the system in attaining that state.
When 56 g of N2 + 10 g of H2 is taken as a
They are inexact differentials whose
combination then dihydrogen (H2 ) act as a
integration gives a total quantity depending
limiting reagent in the reaction.
upon the path.
N2 ( g ) + 3H2 ( g ) ¾® 2NH3 ( g ) …(I)
2 ´ 14g 3 ´ 2g 2(14 + 3 )
Option (a), i.e. q + W and option (d), i.e. H–TS
28g 6g 34g
are state functions. The value of state functions
is independent to the way in which the state is
28g N2 requires 6g H2 gas.
attained. All the state functions are exact
6g
56g of N2 requires ´ 56 g = 12g of H2 differentials and cyclic integration involving a
28 g state functions is zero.
12g of H2 gas is required for 56g of N2 gas but
8 (b) The degenerate orbitals of [Cr(H2O)6 ]3 + are
only 10 g of H2 gas is present in option (a).
dxz and dyz . Electronic configuration of Cr3 + is
Hence, H2 gas is the limiting reagent.
In option (b), i.e. 35g of N2 + 8 g of H2. 3d5 4s1 . The five d-orbitals in an isolated
gaseous atom or ion have same energy, i.e. they
As 28 g N2 requires 6g of H2.
are degenerate. This degeneracy has been
6g
35g N2 requires ´ 35 g H2 Þ 7.5 g of H2. removed due to the ligand electron–metal
28 g
electron repulsions in the octahedral complex
12 ONLINE JEE Main 2019
to yield three orbitals of lower energy, t2g set 12 (d) Cryolite ore (Na3 AlF6 , sodium
and two orbitals of higher energy, eg set. hexafluoroaluminate) contain fluorine while
other given options such as malachite
(e g )
(Cu 2 (CO)3 (OH)2 ), sphalerite ((Zn , Fe)S) and
dx 2–y2 dz2 bauxite (Al 2O3 ) does not contain fluorine.
D0
13 (c) In CuSO4 × 5H2O, one molecule of water is
Free metal ion (t2g)
indirectly connected to Cu. In this molecule,
dxy dxz dyz
four water molecules form coordinate bond
with Cu 2+ ion while one water molecule is
9 (d) The aerosol is a kind of colloid in which
associated with H-bond with SO2- 4 .
solid is dispersed in gas. e.g. smoke, dust.
Structure of CuSO4 × 5H2 O
10 (b) C60 is aromatic allotrope of carbon
containing 12 pentagons and 20 hexagons. It is H H
a fullerene having a shape like soccer ball and d+
d–
called Buckminster fullerene. O O H H O– O
H S
Cu2+ O
11 (a) Key Idea LiAlH4 reagent is used for the reduction of H d– d+ O
O O H H O–
O
½½
¾ CHO, — C OCH3. It does not reduce double bonds. H H
O H
N=
=N —NH2 + HCl
–
CH3CH CH C + CH3O
An aldehyde For an effective coupling, the solution must be
H Nu H– – so alkaline that the concentration of diazonium
cle
op AlH
hili
rea c a 3 s ion is too low. It must not be so acidic that the
cti dd O
on itio
n
concentration of free amine or phenoxide ion is
H+
too low. That is why amines couple fastest in
CH3 CH CH CH2OH H2O
CH3CH CH C H mild acidic solution and phenols couple fastest
Primary alcohol in mild alkaline solution.
H
APRIL ATTEMPT ~ 09 April 2019, Shift I 13
19 (a) Critical temperature is the temperature of Multiplying (i) and (ii) we get
a gas above which it cannot be liquefied what yN xM > yM xN
ever high the pressure may be. The kinetic xM yM
energy of gas molecules above this temperature \ >
xN yN
is sufficient enough to overcome the attractive
forces. It is represented as Tc . Thus, correct relation is (a).
8a
Tc = 23 (c) The IUPAC name of the given compound is
27Rb
8 ´ 13
.
For Ar, Tc = = 0.0144 NO2
27 ´ 8.314 ´ 3.2
4
Incorrect
8 ´ 0.2
Correct
Tc = = 0.0041 3
way
way
For Ne,
27 ´ 8.314 ´ 17
.
2
8 ´ 51
.
For Kr, Tc = = 018
. 1 Cl
27 ´ 8.314 ´ 1.0
8 ´ 41. CH3
For Xe, Tc = = 0.02
27 ´ 8.314 ´ 5.0 2- chloro-1-methy l- 4-nitrobenzene
The value of Tc is highest for Kr (Krypton). Here, the given compound contains two or more
20 (d) The major product obtained in the given functional groups. So, the numbering is done in
reaction is CH3 C (I) (Cl) CHD2. such a way that the sum of the locants is the
1. DCl (1 equiv. ) lowest.
CH3 C ºº CH ¾¾¾¾® CH3 C (I)(Cl)CHD2 24 (d) The effect of release of CO2 gas into
2. DI
atmosphere is global warming.
Addition in unsymmetrical alkynes takes place 25 (c) Optical activity is the ability of a chiral
according to Markovnikov’s rule. molecule to rotate the plane of polarised light,
Reaction proceed as follows : measured by a polarimeter. A chiral molecule
Cl does not have any plane of symmetry. If a
DCl (1 equiv.) ½ DI molecule possess any plane of symmetry, then
CH3 C ºº CH ¾¾¾¾¾® CH3 C == CHD ¾¾ it is an achiral molecule. Given options (a), (b)
Prop-1-yne
and (d) possess plane of symmetry.
Cl
½
CH3 ¾ C ¾ CHD2 A A
½ B
I B
Product en M en
M
21 (a) Magnesium powder burns in air to give MgO B
and Mg3 N2. MgO does not combine with excess B
oxygen to give any superoxide. Mg reacts with
nitrogen to form magnesium nitride (Mg3 N2 ). A
A
Mg + O2 ¾¾® MgO (d)
(b)
3Mg + N2 ¾¾® Mg3 N2
B
22 (a) Key Idea For a solution of volatile liquids the A B
partial vapour pressure of each component of the
solution is directly proportional to its mole fraction M
present in solution. This is known as Raoult’s law.
B A
Liquid M and N form an ideal solution. Vapour
pressures of pure liquids M and N are 450 and
700 mm Hg respectively. A
\ p ºN > p ºM (a)
So, by using Raoult’s law
Only molecule (c) does not possess any plane of
yN > xN …(i) symmetry. Hence, it is a chiral molecule and
and xM > yM …(ii) shows optical activity.
APRIL ATTEMPT ~ 09 April 2019, Shift I 15
26 (d) In first order reaction, the rate expression oxidised to ¾ COOH group irrespective of the
depends on the concentration of one species length of carbon chain.
only having power equal to unity. –+
CH2CH3 COOK COOH
nr ¾® products
- d[r ]
= k [r ] (i) Alk. KMnO4 (ii) H3O+
dt
On integration, - ln[r ] = kt - ln[r0 ]
Ethyl Potassium Benzoic acid
or ln(r ) = ln(r0 ) - kt benzene benzoate
y = c + mx
28 (a) C2 will be stabilised after forming anion.
m = slope = -k (negative)
The electronic configuration of carbon is
c = intercept = ln (r0 ) 1s2 2s2 2 p 2. There are twelve electrons in C2.
The graph for first order reactions is After forming anion (i.e. C–2 ), the electronic
configuration is
-
2 : (s1s) (s 1s) (s 2s) (s * 2s) (p 2 px = p 2 py )
● C
2 * 2 2 2 2 2
1 1
ln (r) Bond order = (Nb - N a ) = (9 - 4) = 2.5
2 2
For other options such as F2- , O-2 , NO- , the
electronic configurations are as follows :
t F2- : (s1s)2 (s* 1s)2 (s2s)2 (s* 2s)2 (s2 pz )2
(p 2 px2 = p 2 py2 ) (p * 2 px2 = p * 2 py2 )(s* 2 p1z )
In zero order reaction,
Bond order = 1 / 2(Nb - N a ) = 1 / 2(10 - 9) = 0.5
[r ] ¾® product
- d[r ]t ● O2- : (s1s)2. (s* 1s)2 (s2s)2 (s* 2s)2 (s2 pz )2
\ = k or - d[r ]t = kdt (p 2 px2 = p 2 py2 ) (p * 2 px2 = p * 2 p1y )
dt
1 1
On integrating, -[r ]t = kt + c Bond order = (Nb - N a ) = (10 - 7) = 15 .
2 2
-
● NO : (s1s)
If t = 0,[r ]t = [r ]0 2
(s 1s) (s 2s) (s * 2s) (s2 pz )2
* 2 2 2
1 1
[r ]t = [r ]0 - kt Bond order = (Nb - N a ) = (10 - 6) = 2
2 2
Thus, the graph plotted between [r ]t and t gives
The value of bond order of C-2 is highest among
a straight line with negative slope (-k ) and
the given options. Bond order between two
intercept equal to [r ]0 .
atoms in a molecule may be taken as an
The graph for zero order reaction is approximate measure of the bond length.
The bond length decreases as bond order
increases. As a result, stability of a molecule
increases.
[r] 29 (b) The correct increasing order of oxidation
state of nitrogen for nitrogen oxides is
+1 +2 +3 +4
N 2 O < NO < N 2 O3 < NO2
● Oxidation state of N in N2O is
t
2(x) - 2 = 0
27 (a) The major product of the given reaction is 2
x = + = +1
benzoic acid (C6 H5 COOH). On vigorous 2
oxidation of alkyl benzene with acidic or ● Oxidation state of N in NO is
alkaline KMnO4 , aromatic acids are obtained. x-2= 0
During oxidation of alkyl benzene, the aromatic x = +2
nucleus remains intact and the entire chain is
16 ONLINE JEE Main 2019
MATHEMATICS
1 (c) Let the slope of line is m, which is passing Now, in DPRQ,
through P (2, 3).
QR = 16 - d 2 = 16 - 2 = 14
Y d 2 1 m+ 1
\tan q = = = =
8 QR 14 7 1- m
é m2 - m1 ù
7 êQ tan q = ú
êë 1 + m1 m2 úû
6
m+ 1 1
5 Þ =±
1- m 7
4 R m+ 1 1 m+ 1 1
d Þ = or =-
3 P (2 , 1- m 7 1- m 7
3)
2 1- 7 -1 - 7
q Þ m= or m =
4 Q 1+ 7 7 -1
1
X¢ X 2 (d) The non-zero four degree polynomial f (x)
1 2 3 4 5 6 7 8 9 has extremum points at x = -1, 0,1, so we can
assume f ¢(x) = a (x + 1)(x - 0) (x - 1) = ax(x2 - 1)
Y¢ x+y=7
where, a is non-zero constant.
Since, the distance of a point (x1 , y1 ) from the f ¢(x) = ax3 - ax
a a
ax1 + by1 + c Þ f (x ) = x 4 - x 2 + C
line ax + by + c = 0 is d = . 4 2
a 2 + b2 [integrating both sides]
\The distance of a point P (2, 3) from the line where, C is constant of integration.
x + y - 7 = 0, is Now, since f (x) = f (0)
|2 + 3 - 7| a 4 a 2 x4 x2
d= Þ x - x +C =C Þ =
1+ 1 4 2 4 2
2 Þ x (x - 2) = 0 Þ x = - 2 , 0, 2
2 2
= = 2
2 Thus, f (x) = f (0) has one rational and two
irrational roots.
APRIL ATTEMPT ~ 09 April 2019, Shift I 17
Now, locus of mid-point M is 10 (b) Key Idea (i) First find the focus of the given
1 1 parabola
+ =4
x2 y2 (ii) Then, find the slope of the focal chord by
Þ x2 + y2 - 4x2 y2 = 0 y - y1
using m = 2
x2 - x1
So, correct option is (c).
8 (c) Given, function f : R – {1, - 1} ® A defined as (iii) Now, find the length of the focal chord by
2
using the formula 4a cosec 2 a.
x
f (x ) = = y (let)
1 - x2 Equation of given parabola is y2 = 16x, its focus
Þ x = y(1 - x2 )
2 2
[Q x ¹ 1] is (4, 0).
Þ x2 (1 + y) = y Since, slope of line passing through (x1 , y1 ) and
y y -y
Þ x2 = [provided y ¹ -1] (x2 , y2 ) is given by m = tan q = 2 1 .
1+ y x2 - x1
Q x2 ³ 0 \ Slope of focal chord having one end point is
y 4- 0 4
Þ ³ 0 Þ y Î (-¥ , - 1) È [0, ¥ ) (1, 4) is m = tan a = =-
1+ y 1- 4 3
Since, for surjective function, range of [where, ‘a’ is the inclination of focal chord with
f = codomain X-axis.]
\Set A should be R - [-1, 0). Since, the length of focal chord = 4a cosec2a
\ The required length of the focal chord
9 (c) Key Idea Use property of definite integral. = 16 [1 + cot 2 a ]
b b
[Q a = 4 and cosec2a = 1 + cot 2 a ]
òa f ( x) dx = òa f ( a + b - x) dx é 9ù é 1 3ù
= 16 ê1 + ú = 25 units êQ cot a = =- ú
p ë 16 û ë tan a 4û
sin3 x
Let I = ò02 sin x + cos x dx …(i)
11 (a) Given differential equation is
On applying the property, dy
x + 2 y = x2 , (x ¹ 0)
b b dx
òa f (x)dx = òa f (a + b - x) dx, we get dy æ 2 ö
Þ + ç ÷ y = x,
cos3 x
p/2 dx è x ø
I= ò0
cos x + sin x
dx …(ii)
which is a linear differential equation of the
On adding integrals (i) and (ii), we get form
3 3
p/ 2 sin x + cos x dy
2I = ò dx + Py = Q
0 sin x + cos x dx
p
(sin x + cos x) (sin 2 x + cos2 x - sin x cos x) 2
= ò2 dx Here, P = and Q = x
0 sin x + cos x x
2
p
é 1 ù ò dx
= ò 2 ê1 - (2 sin x cos x)ú dx \ IF = e x = e2 log x = x2
0 ë 2 û
Since, solution of the given differential equation is
p
æ 1 ö y ´ IF = ò (Q ´ IF) dx + C
= ò
2ç 1 -
0è 2
sin 2x ÷ dx
ø
x4
é 1 ù
p/ 2
\ y(x2 ) = ò (x ´ x2 ) dx + C Þ yx2 = +C
= ê x + cos 2xú 4
ë 4 û0 1 3
æ p ö 1 Q y(1) = 1, so 1 = + C ÞC =
= ç - 0 ÷ + (-1 - 1) 4 4
è2 ø 4 x 4
3
p 1 \ yx2 = +
= - 4 4
2 2 2
x 3
p 1 p -1 Þ y= +
Þ I= - = 4 4x2
4 4 4
APRIL ATTEMPT ~ 09 April 2019, Shift I 19
2 4
On applying R1 ® R1 + R2 + R3 , we get dx
27 (b) Let I = ò sec3 x cos ec3 x dx = ò
y + 1+ a + b y + 1+ a + b y + 1+ a + b 2 4
dx cos3 x sin 3 x
D= a y+b 1
ò 4
b 1 y+ a æ sin x ö3
4 2
ç ÷ 3 3
y y y ç cos x ÷ cos x cos x
è ø
= a y+b 1 [Q a + b = -1] [dividing and multiplying by cos4/3 x
b 1 y+ a in denominator]
On applying C2 ® C2 - C1 and C3 ® C3 - C1 , dx sec2 x dx
we get
= ò 4
= ò 4
For intersecting points A and B 29 (a) Key Idea Use the formula of sum of first n terms
n
Taking, x2 = x + 2 Þ x2 - x - 2 = 0 of AP, i.e Sn = [2 a + ( n - 1) d ]
2
Þ x2 - 2x + x - 2 = 0
Given AP, is
Þ x(x - 2) + 1(x - 2) = 0
a1 , a2 , a3 ,… having sum of first n-terms
Þ x = -1, 2 Þ y = 1, 4 n
So, A(-1, 1) and B (2, 4). = [2a1 + (n - 1)d ]
2
2
[where, d is the common difference of AP]
ò [(x + 2) - x
2
Now, shaded area = ] dx
n (n - 7)
-1 = 50n + A (given)
2 2
é x2 x3 ù æ4 8ö æ 1 1ö
= ê + 2x - ú = ç + 4 - ÷ - ç - 2 + ÷ 1 n-7
3 û -1 è 2 3ø è 2 3ø Þ [2a1 + (n - 1)d ] = 50 + A
ë2 2 2
1 9 1 1 9
= 8 - - = 8 - - 3 = 5 - = sq units 1 æ 7 ö n
2 3 2 2 2 Þ [2a + nd - d ] = ç 50 - A ÷ + A
2 1 è 2 ø 2
APRIL ATTEMPT ~ 09 April 2019, Shift I 23
æ d ö nd æ 7 ö n ® ®
Q b 2 is perpendicular to a, so b 2× a = 0
Þ ç a1 - ÷ + = ç 50 - A ÷ + A
è 2ø 2 è 2 ø 2
[since if non-zero vectors a and b are
On comparing corresponding term, we get perpendicular to each other, then a × b = 0]
d 7
d = A and a1 - = 50 - A \ (3l - 2)(3) + (l + 1)(1) = 0
2 2
Þ 9l - 6 + l + 1 = 0
A 7
Þ a1 - = 50 - A [Q d = A] Þ 10l = 5
2 2 1
Þ l=
Þ a1 = 50 - 3A 2
So a50 = a1 + 49d ® 3$ 1$
So, b1 = i + j
2 2
= (50 - 3A ) + 49A [Q d = A]
® æ3 ö æ1 ö
= 50 + 46A and b 2 = ç - 2 ÷ $i + ç + 1÷ $j - 3k
$
è2 ø è2 ø
Therefore, (d , a50 ) = (A , 50 + 46A ) 1 3
= - $i + $j - 3k $
® ® 2 2
30 (b) Given vectors a = 3$i + $j and b = 2$i - $j + 3k
$
® ® ® $j $
and b = b1 - b 2 $i k
® ® 3 1
® ® ® \b 1 ´ b 2 = 0
such that b1 is parallel to a and b 2 is 2 2
-1 3 -3
perpendicular to a
® 2 2
So, b 1 = la = l(3$i + $j) æ 3 ö æ 9 ö $ æ 9 1ö
® ® ®
= i ç - - 0 ÷ - $jç - - 0 ÷ + k
$
ç + ÷
Now, b 2 = b1 - b = l(3$i + $j) - (2$i - $j + 3k
$) è 2 ø è 2 ø è 4 4ø
3$ 9$ 5 $ 1
$ $
= (3l - 2)i + (l + 1) j – 3k $ = - i + j + k = (-3i + 9$j + 5k
$ $)
2 2 2 2