Unique Set. 03
Unique Set. 03
.√ .√
−y = √
+ ; wbY©q Kivi Rb¨ 02 b¤^i| 02 marks for determining, −y = √
+
−2x y = 2x y + xy + + xy − y ; wbY©q Kivi Rb¨ 02 b¤^i| 02 marks for determining, −2x y = 2x y + xy + +
4x y + 4xy − (1 − 4x )y = 0 ; ‡`Lv‡bvi Rb¨ 04 b¤^i| xy − y
04 marks for showing, 4x y + 4xy − (1 − 4x )y = 0
πr h = 1 ⇒ 2rh + r =0⇒ =−
Avevi, A = 2πr (r + h) ∴ = 2π(r + h) + 2πr 1 +
=0 ⇒r+h+ 1− r = 0 ⇒ r + h + r − 2h = 0 Again, A = 2πr (r + h) ∴ = 2π(r + h) +
2πr 1 + =0⇒r+h+ 1− r=0⇒r+h+
⇒ h = 2r ∴ 2πr = 1 ⇒ r = 0.542 dm = 5.42 cm এবং
h = 2r = 1.084 dm = 10.84 cm [Ans.] r − 2h = 0
∴ x + y = a … (i) ∴ x + y = a … (i)
GLb, x + y = a Now, x + y = a
⇒ x + y =0⇒ = ⇒ x + y =0⇒ =
⇒ yy − y = −x x + x ⇒ yy − y = −x x + x
⇒ yy + xx =a ⇒ yy + xx =a
⇒ + =1 ⇒ + =1
tangent at point (𝑥 , 𝑦 ), is 𝑚 =
¯úk©‡Ki mgxKiY, yy + xx = a ; wbY©q Kivi Rb¨ 03 b¤^i|
KwZ©Z As‡ki e‡M©i †hvMdj = 𝑎 = aªæeK ; †`Lv‡bvi Rb¨ 04 b¤^i| 03 marks for determining, equation of tangent,
yy + xx =a
04 marks for showing, sum of the squares of the
intercept parts = 𝑎 = Constant
2 2
0 4 3 0 4 3
tan x , 0 ≤ x ≤ tan x , 0 ≤ x ≤
y= y=
cot x , ≤ x ≤ cot x , ≤ x ≤
x = ⇒x +x −2 =0 x = ⇒x +x −2 =0
⇒ (x + 2)(x − 1) = 0 ∴ x ∈ ℝ ⇒ (x + 2)(x − 1) = 0 ∴ x ∈ ℝ
∴ x = ±1 ∴ x = ±1
∴ †ÿÎdj = 2 ∫ −x dx ∴ Area = 2 ∫ −x dx
c`v_©weÁvb Phy
01 [Medium] 10
Bqs Gi wØwPo cixÿvq `ywU wP‡oi ga¨eZx© `~iZ¡ 2mm| Av‡jvi Zi½‰`N©¨ In Young's double-slit experiment, the distance between the
600 nm Ges c`©v n‡Z wPo؇qi `~iZ¡ 2m| hw` †K›`ªxq Pi‡gi ZxeªZv two slits is 2 mm. The wavelength of light is 600nm, and
0.2 Wm nq Z‡e, †K›`ªxq D¾¡j †Wviv n‡Z 0.5 cm `~i‡Z¡ ZxeªZv the distance from the slits to the screen is 2 m. If the
KZ? intensity at the central maximum is 0.2 Wm , what is the
intensity at a point 0.5 cm away from the central bright
fringe?
. × × × . × × ×
c_ cv_©K¨, ∆x = = = 5 × 10 m Path difference, ∆x = = = 5 × 10 m
∆ ∆
`kv cv_©K¨, Q = = Phase difference, Q = =
A = A + A + 2A cos =A A = A + A + 2A cos =A
A = √A + A + 2A = √4A = 2A A = √A + A + 2A = √4A = 2A
=( )
⇒ I = × 0.2 =( )
⇒ I = × 0.2
I = 0.05 Wm I = 0.05 Wm
c`v_©weÁvb Phy
02 10
GKwU AceZ©b †MÖwUs G cÖwZ 10 𝑐𝑚 G 7000 †iLv Av‡Q| †MÖwUs n‡Z In a diffraction grating, there are 7000 lines per 10 cm.
c`©vi `~iZ¡ 750 𝑐𝑚| me©wb¤œ KZ †KŠwYK `~i‡Z¡ 340 𝑛𝑚 Ges Distance of the screen from the grating is 750 cm. What
453.33 𝑛𝑚 Zi½‰`‡N©¨i `ywU Av‡jvi Rb¨ Pig GKB ¯’v‡b cvIqv hv‡e? should be the minimum angular distance at which the
maximum of two lights of wavelength 340 nm and 453.33
nm will be found at a same place?
sin 𝜃 = 𝑛 𝑁𝜆 = 𝑛 𝑁𝜆 ⇒ = = 1.333 ≈ sin 𝜃 = 𝑛 𝑁𝜆 = 𝑛 𝑁𝜆 ⇒ = = 1.333 ≈
∴ 𝑛 = 4, 𝑛 = 3 ∴ 𝑛 = 4, 𝑛 = 3
∴ sin 𝜃 = 4 × 70000 × 340 × 10 ⇒ 𝜃 = 5.463 [Ans.] ∴ sin 𝜃 = 4 × 70000 × 340 × 10 ⇒ 𝜃 = 5.463 [Ans.]
c`v_©weÁvb Phy
03 [Easy] 10
A‡bK¸‡jv mgeZ©K dvwj cici GKmv‡_ ¯’vcb Kiv n‡jv †hb †h‡Kv‡bv Several parallel polarizers are arranged serially such that
GKwU dvwji Av‡jvK Aÿ Zvi cv‡ki Av‡jvK A‡ÿi mv‡_ 15° †KvY K‡i the polarization axis of each polarizer makes a 15° angle
_v‡K| Gfv‡e A‡bK¸wj dvwj cici mvRv‡bv n‡jv hZÿY bv †kl dvwjwU with the adjacent one. This setup continues until the last
1g dvwji mv‡_ 90° †KvY Drcbœ K‡i| Gevi 1g dvwj w`‡q 1.2 × 10 polarizer forms a 90° angle with the first. If an unpolarized
jv· ZxeªZvi GKwU AmgewZ©Z Av‡jv cÖ‡ek Ki‡j †kl dvwj w`‡q KZ light of intensity 1.2 × 10 lux enters through the first
ZxeªZvi Av‡jv wbM©Z n‡e? polarizer, what is the intensity of light emerging from the
last polarizer?
†gvU dvuwj cÖ‡qvRb = + 1 = 7wU| Total polarizers needed = + 1 = 7nos
. × . ×
I = (cos 15°) = × (0.933) = 3.958 × 10 I = (cos 15°) = × (0.933) = 3.958 × 10
jv·| lux.
c`v_©weÁvb Phy
04 [Medium] 10
†Kv‡bv e„ËvKvi cÖ¯’‡”Q‡`i cwievnx Zv‡ii GKK AvqZ‡b 4.8 × 10 wU A conductive wire of circular cross-section has 4.8 ×
e Av‡Q| d‡Uv B‡jKwUªK †Kvl Drm †_‡K ZviwU‡Z 1.6A Zwor cÖevwnZ 10 nos electrons per unit volume. When connected to a
n‡”Q| †Kv‡l AvcwZZ Av‡jvi Zi½‰`N©¨ 300 nm Ges wbM©Z d‡Uv photoelectric cell, it produces a current of 1.6A.
B‡jKUª‡bi †e‡Mi 0.0004% †e‡M cwievnx‡Z cwievnx e QzU‡Q| Zv‡ii Wavelength of light incident on the cell is 300nm. If the
cÖ¯’‡”Q‡`i ‡ÿÎdj KZ? [λ = 350 nm, a‡iv, me¸‡jv e Zwor velocity of conduction electrons is 0.0004% of the velocity
of photoelectrons, what is the cross-sectional area of the
cÖev‡n Ask †bq]
wire? [λ = 350 nm, assume all electrons contribute to the
current flow]
= + mv = + mv
c`v_©weÁvb Phy
06 [Easy] 10
GKwU †Uª‡bi wbðj ˆ`N©¨ 250m| GKwU e¨w³‡K †UªbwU 6.5 × A train of rest length 250m passes an observer at a relative
10 ms Av‡cwÿK †e‡M AwZµg Ki‡Z †UªbwUi KZ mgq jvM‡e? velocity of 6.5 × 10 ms . How much time will it take
[e¨w³i wn‡m‡e] (according to the observer) for the train to pass?
V= V=
. × . ×
× ×
× ×
⇒t = = = = 3.755 μs ⇒t = = = = 3.755 μs
. × . ×
imvqb Chem
01 10
A †hŠMwU‡K (0 − 5)°C ZvcgvÎvq NaNO I HCl Gi mv‡_ wewµqv Kiv‡j Compound ‘B’ is produced when compound ‘A’ reacts
‘B’ †hŠM Drcbœ nq| ‘B’ †hŠMwUi cÖfveKxq wbiæ`‡bi gva¨‡g ‘C’ †hŠM Drcbœ with NaNO and HCl at (0 − 5)°C temperature.
nq| ‘C’ †hŠM 𝐾𝑂𝐻 wgwkÖZ KMnO Gi `ªeY‡K eY©nxb K‡i I †hŠMwU mswkøó Compound ‘C’ is produced by the catalytic dehydration
mg‡MvÎxq †kÖwYi ÿz`ªZg m`m¨| Dchy³ wewµqvmn A, B, C †hŠMmg~n kbv³ of compound ‘B’. Compound ‘C’ decolorizes KMnO
Ki| solution mixed with KOH and the compound is the
smallest member of the concerned homologous series.
Identify compound A, B, C with suitable reactions.
CH CH NH + HNO ⎯⎯⎯⎯⎯⎯⎯⎯ CH CH OH + N + H O CH CH NH + HNO ⎯⎯⎯⎯⎯⎯⎯⎯ CH CH OH + N +
° °
,∆ H O
CH CH OH ⎯⎯⎯⎯⎯ CH = CH + H O ,∆
CH CH OH ⎯⎯⎯⎯⎯ CH = CH + H O
CH = CH + [O] + H O ⎯⎯⎯⎯⎯⎯ CH – CH
| |
CH = CH + [O] + H O ⎯⎯⎯⎯⎯⎯ CH – CH
| |
A → CH CH NH ; B → CH CH OH ; C → CH = CH
A → CH CH NH ; B → CH CH OH ; C → CH = CH
b¤^i eÈb:
A I B †hЇMi mswkøó wewµqv ‡jLvi Rb¨ (02×02) = 04 b¤^i| Mark distribution:
C †hЇMi mswkøó wewµqv ‡jLvi Rb¨ 03 b¤^i| (02 ×02) = 04 marks for writing the reactions
A, B I C kbv³Ki‡Yi Rb¨ (01×03) = 03 b¤^i| concerned with Compound A & B.
[we.`«.t c«fveK/ ZvcgvÎv bv wjL‡j ev fyj wjL‡j 01 b¤^i KZ©b Kiv n‡e|] 03 marks for writing the reactions concerned with
Compound C
(01×03) = 03 marks for identifying A, B & C.
[N.B.: 01 mark will be deducted if temperature/catalyst
is not written or wrong written.]
imvqb Chem
02 10
‘𝐴’ †hŠMwU‡K †mvWvjvB‡gi mv‡_ DËß Ki‡j B †hŠM Drcbœ nq| ‘B’ †hŠMwU‡K MoO When compound ‘A’ reacts with soda lime
cÖfve‡Ki Dcw¯’wZ‡Z Aw·‡R‡bi mv‡_ wewµqvq ‘C’ †hŠM Drcbœ nq| C †hŠM mswkøó †kÖwYi with heated, compound ‘B’ is produced.
ÿz`ªZg m`m¨ Ges 2,4: 𝐷𝑁𝑃 cixÿv †`q| wewµqvmn A, B, C †hŠMmg~n kbv³ Ki| Again, when compound ‘B’ reacts with
Oxygen in presence of the catalyst MoO ,
compound ‘C’ is produced. Compound ‘C’ is
the smallest member the concerned series and
gives 2,4: 𝐷𝑁𝑃 test. Identify the compounds
A, B, C with reaction.
,∆ ,∆
CH COOH + NaOH ⎯⎯⎯ CH + Na CO CH COOH + NaOH ⎯⎯⎯ CH + Na CO
H O NO2
A ⎯⎯ CH COOH N − NH NO + H O
B ⎯⎯ CH A ⎯⎯ CH COOH
C ⎯⎯ HCHO B ⎯⎯ CH
C ⎯⎯ HCHO
b¤^i eÈb:
Mark distribution:
A I B †hЇMi mswkøó wewµqv ‡jLvi Rb¨ (02×02) = 04 b¤^i|
(02 ×02) = 04 marks for writing the reactions
C †hЇMi mswkøó wewµqv ‡jLvi Rb¨ 03 b¤^i| concerned with Compound A & B.
A, B I C kbv³Ki‡Yi Rb¨ (01×03) = 03 b¤^i| 03 marks for writing the reactions concerned
[we.`«.t c«fveK/ ZvcgvÎv bv wjL‡j ev fyj wjL‡j 01 b¤^i KZ©b Kiv n‡e|] with Compound C
(01×03) = 03 marks for identifying A, B & C.
[N.B.: 01 mark will be deducted if
temperature/catalyst is not written or wrong
written.]
imvqb Chem
03 10
Dchy³ wewµqvi mvnv‡h¨ wb‡¤œv³ iƒcvšÍimg~n m¤úbœ Ki: Complete the following conversions with the help of
(a) wg_vbwqK GwmW †_‡K B_¨vb¨vj| suitable reactions:
(b) A¨vwmUvjwWnvBW †_‡K †µv‡Uvb¨vjwWnvBW| (a) Ethanal from methanoic acid.
(b) Crotonaldehyde from acetaldehyde.
(a) HCOOH + Ca ⎯⎯ (HCOO) Ca + H (a) HCOOH + Ca ⎯⎯ (HCOO) Ca + H
∆ ∆
(HCOO) Ca + (CH COO) Ca → 2CH CHO + 2CaCO (HCOO) Ca + (CH COO) Ca → 2CH CHO + 2CaCO
(a) (a)
weKí: 01 Alternative: 01
HCOOH ⎯⎯⎯ CH OH ⎯ CH Cl ⎯ CH CN
HCOOH ⎯⎯⎯ CH OH ⎯ CH Cl ⎯ CH CN
,
⎯⎯⎯⎯ CH COOH ⎯⎯⎯ CH CHO ,
∆
⎯⎯⎯⎯ CH COOH ⎯⎯⎯ CH CHO
∆
(a) weKí : 02
(a) Alternative: 02
2HCOOH ⎯⎯⎯ 2HCHO ⎯⎯⎯ 2CH OH ⎯
[ ] [ ] 2HCOOH ⎯⎯⎯ 2HCHO ⎯⎯⎯ 2CH OH ⎯
[ ] [ ]
সূযােলাক (িনয়ি ত)
2CH Cl ⎯⎯⎯⎯⎯⎯ CH CH ⎯⎯⎯⎯⎯⎯⎯⎯⎯
2CH Cl ⎯⎯⎯⎯⎯⎯ CH CH ⎯⎯⎯⎯
( ) [ ]
CH CH Cl ⎯⎯⎯⎯⎯ CH CH OH ⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯ ( ) [ ]
∆ CH CH Cl ⎯⎯⎯⎯⎯ CH CH OH ⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯
∆
CH CHO
CH CHO
লঘু
(b) 2CH CHO ⎯⎯⎯⎯⎯⎯ CH − CH − CH − CHO (b) 2CH CHO ⎯⎯⎯⎯⎯⎯ CH − CH − CH − CHO
|
|
∆ ∆
CH − CH − CH − CHO → CH − CH = CH − CHO + H O CH − CH − CH − CHO → CH − CH = CH − CHO +
| |
H O
imvqb Chem
04 10
wb‡¤œi wewµqv¸‡jv m¤ú~Y© Ki: Complete the following reactions:
NH2 NH2
NHCH3 NHCH3
(ii) +HNO ⎯⎯⎯⎯⎯⎯⎯ +H O (ii) +HNO ⎯⎯⎯⎯⎯⎯⎯ +H O
NH2 NH2
(iii) ⎯⎯ +H O (iii) ⎯⎯ +H O
NH2 NH2
N C N C
(iv) + + → +KCl + H O (iv) + + → +KCl + H O
HO HO
(i) +N (i) +N
CH3 N N O CH3 N N O
(ii) (ii)
NO2 NO2
(iii) (iii)
imvqb Chem
05 10
GKwU †hЇMi bgybv `ªe‡Y eªvwWi weKviK †hvM Ki‡j njy` Aat‡¶c c‡o| Z‡e Addition of Brady's reagent to a sample solution of a
D³ †hŠM wmd weKvi‡Ki mv‡_ wewµqv K‡i bv| wK¬‡gbmb weRvi‡Y GwU compound gives yellow precipitate. However, the
†c‡›Ub Drcbœ K‡i Ges n¨v‡jvdig wewµqvq Ask †bq| bgybv †hŠMwUi compound does not react with Schiff's reagent. It
IUPAC c×wZ‡Z bvg, ms‡KZ Ges Zxeª Rvi‡Y cÖvß cÖavb Drcv`mg~n wjL| produces pentane in Clemmensen reduction and
participates in haloform reactions. Write down the name
in IUPAC method, the formula and the major products
obtained from the strong oxidation of the sample
compound.
|| || ||
m¤¢ve¨ CH − C − CH − CH − CH , CH − CH − C − Between probable CH − C − CH − CH − CH , CH −
CH − CH Gi g‡a¨ cª_gwU n¨v‡jvdig wewµqv †`q| ||
CH − C − CH − CH the first one of these gives the
|| haloform reaction.
So, Ans: CH − C − CH − CH − CH ; †c›Uvb-2-Ib
||
[ ]
𝐶𝐻 𝐶𝑂𝐶𝐻 𝐶𝐻 𝐶𝐻 𝐶𝐻 𝐶𝑂𝑂𝐻 + 𝐶𝐻 𝐶𝐻 𝐶𝑂𝑂𝐻 So, Ans: CH − C − CH − CH − CH ; Pentan-2-one
[ ]
𝐶𝐻 𝐶𝑂𝐶𝐻 𝐶𝐻 𝐶𝐻 𝐶𝐻 𝐶𝑂𝑂𝐻 + 𝐶𝐻 𝐶𝐻 𝐶𝑂𝑂𝐻
b¤^i eÈbt
wmd weKvi‡Ki mv‡_ K‡i bv → wK‡Uvb ‡jLvi Rb¨ 01 b¤^i|
wK¬‡gbm‡b †c‡›Ub nq → C-5 msL¨v wewkó wK‡Uvb ‡jLvi Rb¨ 01 b¤^i| Mark distribution:
01 mark for writing it does not give reaction with Schiff's
||
→ ketone.
CH − C − CH − CH − CH ‡hŠMwU n¨v‡jvdig wewµqv †`q ‡jLvi
01 mark for writing pentane in Clemenson reaction → 5-
Rb¨ 02 b¤^i|
C ketone.
†hЇMi ms‡KZ ‡jLvi Rb¨ 02 b¤^i|
||
†hЇMi IUPAC bvg ‡jLvi Rb¨ 02 b¤^i|
02 marks for writing CH − C − CH − CH − CH gives
bgybv †hŠMwUi Zxeª Rvi‡Y cÖvß cÖavb Drcv`mg~n
haloform reaction.
𝐶𝐻 𝐶𝑂𝑂𝐻, 𝐶𝐻 𝐶𝐻 𝐶𝑂𝑂𝐻 ‡jLvi Rb¨ 02 b¤^i| 02 marks for writing the structural formula.
02 marks for writing the name of compound in IUPAC
method.
02 marks for writing the major products obtained
𝐶𝐻 𝐶𝑂𝑂𝐻, 𝐶𝐻 𝐶𝐻 𝐶𝑂𝑂𝐻 from the strong oxidation of
the sample compound.
imvqb Chem
06 10
GKwU j¨ve‡iUwi‡Z †j‡ejwenxb wZbwU †evZ‡j B_vbj, B_vb¨vj I B_vbwqK In a laboratory, Ethanol, Ethanal and Ethanoic acid is kept in
GwmW i‡q‡Q| Dchy³ wewµqvmn †`LvI †h, wKfv‡e m‡e©v”P `ywU weKviK three unlabeled bottles. How can identify these three
e¨envi K‡i †hŠM¸‡jv kbv³ Kiv hvq| compounds using maximum two reagents. Show with
reactions.
B_vbwqK GwmW Ges B_vbj 2,4-𝐷𝑁𝑃𝐻 Gi mv‡_ †Kv‡bv wewµqv K‡i bv| Ethanoic acid and Ethanol don't react with 2, 4-DNPH,
A_ev, 𝐎𝐫,