Chemistry booster series
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A. Diborane has two 3-centre-2-electron bonds
B. All Bโ€“H bonds in diborane are equivalent
C. Boranes are electron-deficient compounds
D. Terminal Bโ€“H bonds are longer than bridge Bโ€“H bonds
๐Ÿ‘‰ Correct option(s):
1๏ธโƒฃ A and C
2๏ธโƒฃ A, B and C
3๏ธโƒฃ B and D
4๏ธโƒฃ A, C and D


Identify the correct set regarding trihalides of Group 13:
A. Lewis acidity of BXโ‚ƒ decreases from BFโ‚ƒ to BIโ‚ƒ
B. BFโ‚ƒ is a weaker Lewis acid than BClโ‚ƒ
C. AlClโ‚ƒ acts as a Lewis acid
D. Boron trihalides undergo hydrolysis except BFโ‚ƒ
๐Ÿ‘‰ Correct option(s):
1๏ธโƒฃ A and C
2๏ธโƒฃ B, C and D
3๏ธโƒฃ A, B and D
4๏ธโƒฃ B and C only

Identify the correct statements:
A. Bโ‚‚Oโ‚ƒ is acidic in nature
B. Alโ‚‚Oโ‚ƒ is amphoteric
C. Tlโ‚‚Oโ‚ƒ is basic in nature
D. Basic character of oxides decreases down the group
๐Ÿ‘‰ Correct option(s):
1๏ธโƒฃ A and B
2๏ธโƒฃ A, B and C
3๏ธโƒฃ B and D
4๏ธโƒฃ A, C and D
๐Ÿ˜7โค5๐Ÿ’ฏ2๐Ÿ•Š1
thermodynamics.aac
1.6 MB
Topic cover thermodynamics system surrounding boundaries
Intensive extensive property & sign uses
โค9โคโ€๐Ÿ”ฅ5๐Ÿ˜1
Chemistry booster series
Question 1 Identify the correct set of statements related to Group 13 elements: A. Boron shows anomalous behaviour in its group B. Aluminium forms Alยณโบ ion easily in aqueous solution C. Gallium has lower melting point than aluminium D. Inert pair effect increasesโ€ฆ
โœ… Answer: Option 1 (A, C and D)
Boron anomalous โœ”
Alยณโบ strongly hydrated โ†’ aqueous me stable nahi โŒ
Ga ka m.p. Al se kam โœ”
Inert pair effect down the group increase โœ”

โœ… Answer: Option 2 (A, C and D)
BClโ‚ƒ = strong Lewis acid โœ”
AlClโ‚ƒ vapour phase me dimer (Alโ‚‚Clโ‚†) โŒ
Diborane = electron deficient โœ”
Boric acid monobasic โœ”


โœ… Answer: Option 1 (A, B and C)
+3 down the group unstable โœ”
+1 stable due to inert pair โœ”
Tlยณโบ easily reduce hota โ‡’ strong oxidiser โœ”
Boron Bยณโบ ion nahi banata โŒ
๏ปฟ
โค8๐Ÿฅฐ2๐Ÿณ1๐Ÿ†1
Chemistry booster series
A. Diborane has two 3-centre-2-electron bonds B. All Bโ€“H bonds in diborane are equivalent C. Boranes are electron-deficient compounds D. Terminal Bโ€“H bonds are longer than bridge Bโ€“H bonds ๐Ÿ‘‰ Correct option(s): 1๏ธโƒฃ A and C 2๏ธโƒฃ A, B and C 3๏ธโƒฃ B and D 4๏ธโƒฃ A,โ€ฆ
โœ… Answer: Option 1 (A and C)
Diborane me 2 banana bonds โœ”
Terminal & bridge bonds same nahi โŒ
Boranes electron-deficient โœ”
Bridge bonds longer hote hain โŒ

โœ… Answer: Option 2 (B, C and D)
Lewis acidity: BFโ‚ƒ < BClโ‚ƒ < BBrโ‚ƒ < BIโ‚ƒ โœ”
AlClโ‚ƒ = Lewis acid โœ”
BFโ‚ƒ hydrolysis nahi karta โŒ (others karte)
A statement ulta likha โŒ

โœ… Answer: Option 2 (A, B and C)
Bโ‚‚Oโ‚ƒ acidic โœ”
Alโ‚‚Oโ‚ƒ amphoteric โœ”
Tlโ‚‚Oโ‚ƒ basic โœ”
Basic character increase hota hai down the group โŒ
๐Ÿ˜Ž4๐Ÿ˜3๐Ÿ‘Œ1
#ELECTROMAGNETICRADIATION
Electromagnetic radiation is a form of energy propagated as waves with electric and magnetic fields oscillating perpendicular to each other.

#๏ธโƒฃ 1๏ธโƒฃ Characteristics of EM Radiation

โญ Wave Nature
โœ”๏ธ Travels in space as waves
โœ”๏ธ Characterized by wavelength (ฮป), frequency (ฮฝ), speed (c)
โœ”๏ธ Relationship: c = ฮปฮฝ

โญ Particle Nature
โœ”๏ธ Light also behaves as particles (photons)
โœ”๏ธ Energy of photon: E = hฮฝ
โœ”๏ธ Momentum of photon: p = h/ฮป
๐Ÿ“Œ Constants
โœ”๏ธ h = Planckโ€™s constant = 6.626 ร— 10โปยณโด Jยทs
โœ”๏ธ c = speed of light = 3 ร— 10โธ m/s

๐Ÿ“Œ Constants
โœ”๏ธ h = Planckโ€™s constant = 6.626 ร— 10โปยณโด Jยทs
โœ”๏ธ c = speed of light = 3 ร— 10โธ m/s

2#TypesofElectromagneticRadiation (NCERT)
๐Ÿ“Œ Order of increasing wavelength / decreasing frequency:
ฮณ-rays < X-rays < UV < Visible < IR < Microwaves < Radio waves
โœ”๏ธ UV, Visible, IR โ†’ Important in Atomic Spectra

3๏ธโƒฃ #ImportantRelations (Atom Chapter)
โœ”๏ธ Energy of photon: E = hฮฝ = hc/ฮป
โœ”๏ธ Frequency & wavelength inversely proportional: ฮฝ = c/ฮป

4๏ธโƒฃ #NEETIMPORTANTPOINTS โญ
โœ”๏ธ EM radiation has dual nature โ†’ wave + particle
โœ”๏ธ Wave nature โ†’ explains interference, diffraction, refraction
โœ”๏ธ Particle nature โ†’ explains photoelectric effect, Compton effect
โœ”๏ธ Photon energy proportional to frequency (E โˆ ฮฝ)

@Ayano1me @Neetugpoll @Neetugquiz
โค5๐Ÿ‘3๐Ÿ†1
#PBLOCK ELEMENTSGROUP 14 (CARBON FAMILY)
Elements: C, Si, Ge, Sn, Pb
โœ”๏ธ General electronic configuration: nsยฒ npยฒ
โœ”๏ธ Valency: 4
โœ”๏ธ Oxidation states: +4, +2
๐Ÿ“Œ Stability of +2 state increases down the group (inert pair effect)


1๏ธโƒฃ #PHYSICALPROPERTIES
โญ Atomic & Ionic Radii
โœ”๏ธ Increases down the group (C < Si < Ge < Sn < Pb)
โญ Ionisation Enthalpy
โœ”๏ธ Decreases down the group
๐Ÿ“Œ Carbon has very high IE โ†’ strong covalent bonding
โญ Electronegativity
โœ”๏ธ Decreases down the group
๐Ÿ“Œ C highest, Pb lowest
โญ Catenation (NEET HOT ๐Ÿ”ฅ)
โœ”๏ธ Ability to form long chains
๐Ÿ“Œ Order: C >> Si > Ge > Sn > Pb
๐Ÿ“Œ Strong Cโ€“C bond + small size


2๏ธโƒฃ #ALLOTROPY
โญ Carbon Allotropes
โœ”๏ธ Crystalline โ†’ Diamond, Graphite, Fullerene
โœ”๏ธ Amorphous โ†’ Coal, Coke, Charcoal
๐Ÿ“Œ Diamond
โœ”๏ธ spยณ hybridised
โœ”๏ธ Hardest substance
โœ”๏ธ Electrical insulator
๐Ÿ“Œ Graphite
โœ”๏ธ spยฒ hybridised
โœ”๏ธ Good conductor of electricity
โœ”๏ธ Layered structure


3๏ธโƒฃ #CHEMICALPROPERTIES
โญ Oxidation States
โœ”๏ธ C, Si โ†’ mainly +4
โœ”๏ธ Ge, Sn, Pb โ†’ +2 & +4
๐Ÿ“Œ +2 becomes more stable down the group (inert pair effect)
โญ Inert Pair Effect
โœ”๏ธ nsยฒ electrons do not participate in bonding
๐Ÿ“Œ Maximum in Pb โ†’ Pbยฒโบ more stable than Pbโดโบ


4๏ธโƒฃ #HYDRIDES (EHโ‚„)
โœ”๏ธ CHโ‚„, SiHโ‚„, GeHโ‚„, SnHโ‚„
๐Ÿ“Œ Trend:
โœ”๏ธ Thermal stability โ†“ down the group
โœ”๏ธ Reducing character โ†‘ down the group

5๏ธโƒฃ #HALIDES (MXโ‚„ / MXโ‚‚)
โญ Tetrahalides (MXโ‚„)
โœ”๏ธ CClโ‚„, SiClโ‚„ โ†’ covalent
โœ”๏ธ Stability โ†“ down the group
โญ Dihalides (MXโ‚‚)
โœ”๏ธ SnClโ‚‚, PbClโ‚‚ โ†’ more stable down the group
๐Ÿ“Œ Due to inert pair effect
๐Ÿ“Œ PbClโ‚„ unstable, PbClโ‚‚ stable


6๏ธโƒฃ #OXIDES (IMPORTANT ๐Ÿ”ฅ)
โœ”๏ธ COโ‚‚, SiOโ‚‚ โ†’ Acidic
โœ”๏ธ GeOโ‚‚ โ†’ Weakly acidic
โœ”๏ธ SnOโ‚‚ โ†’ Amphoteric
โœ”๏ธ PbO โ†’ Amphoteric / basic

๐Ÿ“Œ Acidity decreases down the group

7๏ธโƒฃ #CARBONSPECIALCASE
โญ Shows maximum catenation
โญ Forms multiple bonds (C=C, Cโ‰กC)
โญ Large number of organic compounds
โญ No d-orbitals โ†’ strong ฯ€ bonding

8๏ธโƒฃ #COMPARISON ( NEET MCQ)
Property :Carbon :Lead
Catenation :Maximum :Negligible
Oxidation state :+4 :+2 more stable
Nature of oxide :Acidic :Amphoteric
Inert pair effect :Absent :Maximum

โš ๏ธ #NCERTLINES
โŒ Pbโดโบ more stable than Pbยฒโบ โ†’ WRONG
โœ”๏ธ CClโ‚„ does NOT hydrolyse
โœ”๏ธ SiClโ‚„ hydrolyses easily
โœ”๏ธ Graphite conducts electricity, diamond does not

@Ayano1me @Neetugpoll @Neetugquiz
โค4๐Ÿ˜2๐Ÿ™1๐Ÿณ1
Chemistry booster series pinned ยซ๐—ง๐—ข๐—ฃ ๐Ÿฎ๐Ÿฌ ๐—›๐—œ๐—š๐—› ๐—ช๐—˜๐—œ๐—š๐—›๐—ง๐—”๐—š๐—˜ ๐—ง๐—ข๐—ฃ๐—œ๐—–๐—ฆ โ€” ๐—–๐—›๐—˜๐— ๐—œ๐—ฆ๐—ง๐—ฅ๐—ฌ โญ #๐—ฃ๐—›๐—ฌ๐—ฆ๐—œ๐—–๐—”๐—Ÿ๐—–๐—›๐—˜๐— ๐—œ๐—ฆ๐—ง๐—ฅ๐—ฌ ๐—–๐—›๐—”๐—ฃ๐—ง๐—˜๐—ฅ ๐Ÿญ: ๐—ฆ๐—ข๐—Ÿ๐—จ๐—ง๐—œ๐—ข๐—ก โญ ๐—œ๐——๐—˜๐—”๐—Ÿ ๐—ฆ๐—ข๐—Ÿ๐—จ๐—ง๐—œ๐—ข๐—ก โญ ๐—–๐—ข๐—Ÿ๐—Ÿ๐—œ๐—š๐—”๐—ง๐—œ๐—ฉ๐—˜ ๐—ฃ๐—ฅ๐—ข๐—ฃ๐—˜๐—ฅ๐—ง๐—œ๐—˜๐—ฆ ๐—–๐—›๐—”๐—ฃ๐—ง๐—˜๐—ฅ ๐Ÿฎ๐—˜๐—Ÿ๐—˜๐—–๐—ง๐—ฅ๐—ข๐—–๐—›๐—˜๐— ๐—œ๐—ฆ๐—ง๐—ฅ๐—ฌ โญ ๐—ก๐—˜๐—ฅ๐—ก๐—ฆ๐—ง ๐—˜๐—ค๐—จ๐—”๐—ง๐—œ๐—ข๐—ก โญ ๐—–๐—ข๐—ก๐——๐—จ๐—–๐—ง๐—œ๐—ฉ๐—œ๐—ง๐—ฌ ๐—–๐—›๐—”๐—ฃ๐—ง๐—˜๐—ฅ ๐Ÿฏ: ๐—–๐—›๐—˜๐— ๐—œ๐—–๐—”๐—Ÿ ๐—ž๐—œ๐—ก๐—˜๐—ง๐—œ๐—–๐—ฆ โญ ๐—™๐—œ๐—ฅ๐—ฆ๐—ง ๐—ข๐—ฅ๐——๐—˜๐—ฅ ๐—ฅ๐—˜๐—”๐—–๐—ง๐—œ๐—ข๐—ก๐—ฆ โญ ๐—”๐—ฅ๐—ฅ๐—›๐—˜๐—ก๐—œ๐—จ๐—ฆโ€ฆยป
Chemistry booster series
๐—ง๐—ข๐—ฃ ๐Ÿฎ๐Ÿฌ ๐—›๐—œ๐—š๐—› ๐—ช๐—˜๐—œ๐—š๐—›๐—ง๐—”๐—š๐—˜ ๐—ง๐—ข๐—ฃ๐—œ๐—–๐—ฆ โ€” ๐—–๐—›๐—˜๐— ๐—œ๐—ฆ๐—ง๐—ฅ๐—ฌ โญ #๐—ฃ๐—›๐—ฌ๐—ฆ๐—œ๐—–๐—”๐—Ÿ๐—–๐—›๐—˜๐— ๐—œ๐—ฆ๐—ง๐—ฅ๐—ฌ ๐—–๐—›๐—”๐—ฃ๐—ง๐—˜๐—ฅ ๐Ÿญ: ๐—ฆ๐—ข๐—Ÿ๐—จ๐—ง๐—œ๐—ข๐—ก โญ ๐—œ๐——๐—˜๐—”๐—Ÿ ๐—ฆ๐—ข๐—Ÿ๐—จ๐—ง๐—œ๐—ข๐—ก โญ ๐—–๐—ข๐—Ÿ๐—Ÿ๐—œ๐—š๐—”๐—ง๐—œ๐—ฉ๐—˜ ๐—ฃ๐—ฅ๐—ข๐—ฃ๐—˜๐—ฅ๐—ง๐—œ๐—˜๐—ฆ ๐—–๐—›๐—”๐—ฃ๐—ง๐—˜๐—ฅ ๐Ÿฎ๐—˜๐—Ÿ๐—˜๐—–๐—ง๐—ฅ๐—ข๐—–๐—›๐—˜๐— ๐—œ๐—ฆ๐—ง๐—ฅ๐—ฌ โญ ๐—ก๐—˜๐—ฅ๐—ก๐—ฆ๐—ง ๐—˜๐—ค๐—จ๐—”๐—ง๐—œ๐—ข๐—ก โญ ๐—–๐—ข๐—ก๐——๐—จ๐—–๐—ง๐—œ๐—ฉ๐—œ๐—ง๐—ฌ ๐—–๐—›๐—”๐—ฃ๐—ง๐—˜๐—ฅ ๐Ÿฏ: ๐—–๐—›๐—˜๐— ๐—œ๐—–๐—”๐—Ÿ ๐—ž๐—œ๐—ก๐—˜๐—ง๐—œ๐—–๐—ฆ โญ ๐—™๐—œ๐—ฅ๐—ฆ๐—ง ๐—ข๐—ฅ๐——๐—˜๐—ฅ ๐—ฅ๐—˜๐—”๐—–๐—ง๐—œ๐—ข๐—ก๐—ฆ โญ ๐—”๐—ฅ๐—ฅ๐—›๐—˜๐—ก๐—œ๐—จ๐—ฆโ€ฆ
Ye vaale sb read kr lena help hogi
Or jo jo topic ka revision ka mood ๐Ÿ˜ถh krlo read
๐Ÿฅฐ4๐Ÿ‘4โคโ€๐Ÿ”ฅ1๐Ÿ’ฏ1
โค5๐ŸŽ‰2๐Ÿ†1
#BOHRMODELOFHYDROGENATOM
Proposed by Niels Bohr (1913) to explain the line spectrum of hydrogen.

1. #POSTULATES OF BOHR MODEL
โœ”๏ธ Atom has a small, positively charged nucleus at the centre
โœ”๏ธ Electron revolves around nucleus in fixed circular orbits (stationary states)
โœ”๏ธ Each orbit has a definite energy
โœ”๏ธ Electron does not radiate energy while revolving in a permitted orbit
๐Ÿ“Œ Allowed orbits โ†’ n = 1, 2, 3, 4โ€ฆ
โœ”๏ธ Angular momentum of electron is quantised:
๐Ÿ“Œ mvr = n(h / 2ฯ€)


2. #ENERGYOFELECTRON IN HYDROGEN ATOM
โœ”๏ธ Energy of electron in nth orbit:
๐Ÿ“Œ Eโ‚™ = โˆ’13.6 / nยฒ eV
โœ”๏ธ Negative sign โ†’ electron is bound to nucleus
๐Ÿ“Œ Ground state (n = 1):
Eโ‚ = โˆ’13.6 eV
๐Ÿ“Œ Excited state (n > 1):
Energy becomes less negative

3. #RADIUSOFBOHRORBIT
โœ”๏ธ Radius of nth orbit:
๐Ÿ“Œ rโ‚™ = 0.529 ร— nยฒ ร…
๐Ÿ“Œ For ground state (n = 1):
rโ‚ = 0.529 ร…
โœ”๏ธ Radius increases as nยฒ

4. #SPECTRALLINES (EMISSION & ABSORPTION)
โœ”๏ธ Electron jumps from higher to lower orbit โ†’ emission of energy
โœ”๏ธ Electron jumps from lower to higher orbit โ†’ absorption of energy
๐Ÿ“Œ Energy difference:
๐Ÿ“Œ ฮ”E = Eโ‚‚ โˆ’ Eโ‚ = hฮฝ


5 #HYDROGENEMISSION SPECTRUM (IMPORTANT )
โœ”๏ธ Spectrum consists of discrete lines
๐Ÿ“Œ Series based on final orbit:
Slines :Final n :Region
Lyman: 1 :UV
Balmer :2 :Visible
Paschen :3 :IR
Brackett :4 :IR
Pfund :5 :IR

๐Ÿ“Œ Balmer series โ†’ only visible series


6. #RYDBERGEQUATION
โœ”๏ธ Explains wavelength of spectral lines:
๐Ÿ“Œ 1/ฮป = R (1/nโ‚ยฒ โˆ’ 1/nโ‚‚ยฒ)
โœ”๏ธ nโ‚‚ > nโ‚
๐Ÿ“Œ R = 1.097 ร— 10โท mโปยน

7. #SUCCESSOFBOHRMODEL
โœ”๏ธ Explains hydrogen line spectrum
โœ”๏ธ Explains stability of hydrogen atom
โœ”๏ธ Gives correct values of energy & radius for H atom


8. #LIMITATIONSOFBOHRMODEL (VERY IMP โš ๏ธ)
โŒ Cannot explain spectra of multi-electron atoms
โŒ Cannot explain Zeeman effect
โŒ Cannot explain Stark effect
โŒ Violates Heisenberg uncertainty principle

9. #NCERT ONELINEFACTS (NEET DIRECT)
โœ”๏ธ Valid only for one-electron systems (H, Heโบ, Liยฒโบ)
โœ”๏ธ Energy levels are quantised
โœ”๏ธ Lower n โ†’ more stability
โœ”๏ธ Higher n โ†’ larger orbit, higher energy

#IMP
Electron radiates energy in stationary orbit โ†’ WRONG
โœ”๏ธ Ground state has minimum energy
โœ”๏ธ Transition n=3 โ†’ n=2 โ†’ Balmer series

@Ayano1me @Neetugpoll @Neetugquiz
โค5โคโ€๐Ÿ”ฅ3๐ŸŽ‰1๐Ÿ’ฏ1๐Ÿ˜Ž1
1๏ธโƒฃ #PBLOCKGROUP15 โญ (Nitrogen Family / Pnictogens)
๐Ÿ“Œ Group members:
โœ”๏ธ Nitrogen (N)
โœ”๏ธ Phosphorus (P)
โœ”๏ธ Arsenic (As)
โœ”๏ธ Antimony (Sb)
โœ”๏ธ Bismuth (Bi)
๐Ÿ“Œ General electronic configuration:
โœ”๏ธ nsยฒ npยณ
NEET point:
โœ”๏ธ 5 valence electrons โ†’ trivalent nature common


2๏ธโƒฃ #GENERALTRENDS โญ
๐Ÿ“Œ Atomic & ionic size:
โœ”๏ธ Increases down the group
๐Ÿ“Œ Ionisation enthalpy:
โœ”๏ธ Decreases down the group
โœ”๏ธ Nitrogen โ†’ highest (small size)
๐Ÿ“Œ Electronegativity:
โœ”๏ธ Decreases down the group
๐Ÿ“Œ Metallic character:
โœ”๏ธ Increases down the group
โœ”๏ธ N & P โ†’ non-metals
โœ”๏ธ As & Sb โ†’ metalloids
โœ”๏ธ Bi โ†’ metal


3๏ธโƒฃ #OXIDATIONSTATES โญ
โœ”๏ธ Common oxidation states: โ€“3, +3, +5
๐Ÿ“Œ Trends:
โœ”๏ธ โ€“3 โ†’ stability decreases down the group
โœ”๏ธ +5 โ†’ stability decreases down the group
โœ”๏ธ +3 โ†’ stability increases down the group
๐Ÿง  Reason:
โœ”๏ธ Inert pair effect increases down the group
๐Ÿ“Œ Examples:
โœ”๏ธ Nโ‚‚Oโ‚… โ†’ +5 (stable)
โœ”๏ธ Biยณโบ โ†’ more stable than Biโตโบ


4๏ธโƒฃ #HYDRIDES (NHโ‚ƒ TYPE) โญ
๐Ÿ“Œ General formula:
โœ”๏ธ EHโ‚ƒ
๐Ÿ“Œ Bond angle:
โœ”๏ธ NHโ‚ƒ > PHโ‚ƒ > AsHโ‚ƒ > SbHโ‚ƒ > BiHโ‚ƒ
๐Ÿ“Œ Basic nature:
โœ”๏ธ NHโ‚ƒ โ†’ most basic
โœ”๏ธ Basicity decreases down the group
Reason:
โœ”๏ธ Lone pair availability decreases
๐Ÿ“Œ Thermal stability:
โœ”๏ธ Decreases down the group


5๏ธโƒฃ #OXIDES โญ
โœ”๏ธ Form Eโ‚‚Oโ‚ƒ and Eโ‚‚Oโ‚…
๐Ÿ“Œ Nature of oxides:
โœ”๏ธ Nโ‚‚Oโ‚…, Pโ‚‚Oโ‚… โ†’ acidic
โœ”๏ธ Asโ‚‚Oโ‚ƒ โ†’ amphoteric
โœ”๏ธ Biโ‚‚Oโ‚ƒ โ†’ basic
Trend:
โœ”๏ธ Acidic โ†’ basic character increases down the group


6๏ธโƒฃ #HALIDES โญ
๐Ÿ“Œ Trihalides (EXโ‚ƒ):
โœ”๏ธ All elements form EXโ‚ƒ
๐Ÿ“Œ Pentahalides (EXโ‚…):
โœ”๏ธ Formed by P, As, Sb
โœ”๏ธ Nitrogen โŒ (no d-orbitals)
โœ”๏ธ Bi โŒ (inert pair effect)
Important:
โœ”๏ธ PClโ‚… โ†’ exists as solid (ionic) & gas (covalent)


7๏ธโƒฃ #ANOMALOUSBEHAVIOUROFNITROGEN โญ
โœ”๏ธ Small size
โœ”๏ธ High electronegativity
โœ”๏ธ High ionisation enthalpy
โœ”๏ธ Absence of d-orbitals
๐Ÿ“Œ Results:
โœ”๏ธ Nโ‚‚ has strong triple bond
โœ”๏ธ Limited oxidation states
โœ”๏ธ Different properties from rest of group


8๏ธโƒฃ #IMPORTANTCOMPOUNDS

โœ”๏ธ Ammonia (NHโ‚ƒ):
โ€ข Basic gas
โ€ข Forms hydrogen bonding

โœ”๏ธ Phosphine (PHโ‚ƒ):
โ€ข Weak base
โ€ข Toxic gas

โœ”๏ธ Pโ‚‚Oโ‚…:
Strong dehydrating agent

#NEETTAKEAWAY
โœ”๏ธ Inert pair effect โ†’ key to oxidation states
โœ”๏ธ NHโ‚ƒ strongest base in group
โœ”๏ธ Acidic โ†’ basic oxide trend important
โœ”๏ธ Nitrogen always exceptional

@Ayano1me @Neetugpoll @Neetugquiz
๐Ÿ”ฅ3๐Ÿ‘Œ3โค1๐Ÿ•Š1๐Ÿ˜1
๐˜พ๐™๐™š๐™ข๐™ž๐™จ๐™ฉ๐™ง๐™ฎ ๐™๐™–๐™ฃ๐™  ๐˜ฝ๐™ค๐™ค๐™จ๐™ฉ๐™š๐™ง ๐™‡๐™€๐™โ€™๐™Ž ๐˜พ๐™๐˜ผ๐˜พ๐™† ๐™„๐™ ๐™‰๐™Š๐™๐™€๐™Ž โš•๏ธ ๐™’๐™–๐™ฎ ๐™ฉ๐™ค ๐™จ๐™ช๐™˜๐™˜๐™š๐™จ๐™จ:
1๏ธโƒฃ #PERIODICCLASSIFICATIONOFELEMENTS โญ
โœ”๏ธ Elements ko increasing atomic number ke order me arrange karna
โœ”๏ธ Purpose โ†’ study of properties in a systematic way
๐Ÿ“Œ Modern periodic law:
โœ”๏ธ Physical & chemical properties of elements are periodic functions of their atomic numbers
#NEETpoint:
โœ”๏ธ Atomic number (Z) is basis, not atomic mass


2๏ธโƒฃ #HISTORICALDEVELOPMENT โญ
โœ”๏ธ Dobereinerโ€™s Triads
โ€ข Middle element mass โ‰ˆ average of other two
โœ”๏ธ Newlandsโ€™ Law of Octaves
โ€ข Every 8th element similar properties
โœ”๏ธ Mendeleevโ€™s Periodic Table
โ€ข Based on atomic mass
โ€ข Left gaps for undiscovered elements
โœ”๏ธ Modern Periodic Table (Moseley)
โ€ข Based on atomic number
#NEETIMP
โœ”๏ธ Anomalies of Mendeleev solved by modern table


3๏ธโƒฃ #MODERNPERIODICTABLE โญ
๐Ÿ“Œ Structure:
โœ”๏ธ 7 periods (horizontal rows)
โœ”๏ธ 18 groups (vertical columns)
๐Ÿ“Œ Blocks:
โœ”๏ธ s-block
โœ”๏ธ p-block
โœ”๏ธ d-block
โœ”๏ธ f-block
#NEETpoint:
โœ”๏ธ Period number = highest principal quantum number (n)


4๏ธโƒฃ #PERIODICITYINPROPERTIES โญ
โœ”๏ธ Repetition of properties at regular intervals
๐Ÿ“Œ Important properties:
โœ”๏ธ Atomic radius
โœ”๏ธ Ionisation enthalpy
โœ”๏ธ Electron affinity
โœ”๏ธ Electronegativity
โœ”๏ธ Metallic & non-metallic character

5๏ธโƒฃ #ATOMICRADIUS โญ
๐Ÿ“Œ Trend:
โœ”๏ธ Decreases across a period โ†’ left to right
โœ”๏ธ Increases down a group
#Reason:
โœ”๏ธ Effective nuclear charge โ†‘ across period
โœ”๏ธ New shell added down the group
๐Ÿ“Œ Ionic radius:
โœ”๏ธ Cation < atom
โœ”๏ธ Anion > atom

6๏ธโƒฃ #IONISATIONENTHALPY โญ
โœ”๏ธ Energy required to remove an electron
๐Ÿ“Œ Trend:
โœ”๏ธ Increases across a period
โœ”๏ธ Decreases down a group
#Exceptions (NEET favourite ๐Ÿ”ฅ):
โœ”๏ธ Be > B
โœ”๏ธ N > O

7๏ธโƒฃ #ELECTRONAFFINITY โญ
โœ”๏ธ Energy released when electron is added
๐Ÿ“Œ Trend:
โœ”๏ธ Increases across a period
โœ”๏ธ Decreases down a group
#NEETpoint:
โœ”๏ธ Halogens โ†’ highest electron affinity
โœ”๏ธ Noble gases โ†’ ~0

8๏ธโƒฃ #ELECTRONEGATIVITY โญ
โœ”๏ธ Tendency to attract shared electron pair
๐Ÿ“Œ Trend:
โœ”๏ธ Increases across a period
โœ”๏ธ Decreases down a group
โญNEETpoint:
โœ”๏ธ Fluorine โ†’ most electronegative

9๏ธโƒฃ #METALLICCHARACTER โญ
๐Ÿ“Œ Trend:
โœ”๏ธ Decreases across a period
โœ”๏ธ Increases down a group
โญNEETclarity:
โœ”๏ธ Metals โ†’ lose electrons
โœ”๏ธ Non-metals โ†’ gain electrons

๐Ÿ”Ÿ #ANOMALOUSBEHAVIOUR โญ
โœ”๏ธ First element of each group shows different properties
๐Ÿ“Œ Reason:
โœ”๏ธ Small size
โœ”๏ธ High electronegativity
โœ”๏ธ Absence of d-orbitals
โญExample:
โœ”๏ธ Li โ‰  Na
โœ”๏ธ Be โ‰  Mg

1๏ธโƒฃ1๏ธโƒฃ #NEETONELINERS๐Ÿ”ฅ
โœ”๏ธ Basis of modern periodic table โ†’ atomic number
โœ”๏ธ Periodicity due to electronic configuration
โœ”๏ธ s-block โ†’ highly electropositive
โœ”๏ธ p-block โ†’ variable oxidation states
โœ”๏ธ d-block โ†’ transition elements

1๏ธโƒฃ2๏ธโƒฃ #SUMMARY โญ
โœ”๏ธ Periodic table = map of chemistry
โœ”๏ธ Trends help predict properties
โœ”๏ธ Exceptions are more important for NEET

@Ayano1me @Neetugpoll @Neetugquiz
โค4๐Ÿ•Š2๐ŸŽ‰1๐Ÿคฉ1๐Ÿ™1๐Ÿ’˜1
Q1. (Assertionโ€“Reason type)
Assertion (A): Atomic radius generally decreases from left to right in a period.
Reason (R): Nuclear charge increases while number of shells remains same.
Options:
(1) A & R both true and R is correct explanation
(2) A & R both true but R is not correct explanation
(3) A true, R false
(4) A false, R true


Q2.
Which element has maximum electronegativity?
(1) Oxygen
(2) Nitrogen
(3) Fluorine
(4) Chlorine


Question:3 Which of the following has largest atomic size?
(1) Na
(2) Mg
(3) Al
(4) Si

Question 4
Assertion (A): Ionization enthalpy generally increases from left to right in a period.
Reason (R): Atomic size decreases and nuclear charge increases across a period.
(1) A & R both true and R is correct explanation
(2) A & R both true but R is not correct explanation
(3) A true, R false
(4) A false, R true


Question:5
Assertion (A): Electron affinity of halogens is high.
Reason (R): Halogens have one electron less than noble gas configuration.
(1) A & R both true and R is correct explanation
(2) A & R both true but R is not correct explanation
(3) A true, R false
(4) A false, R true

Question:6
Assertion (A): Metallic character increases down a group.
Reason (R): Atomic size increases and ionization enthalpy decreases down the group.
(1) A & R both true and R is correct explanation
(2) A & R both true but R is not correct explanation
(3) A true, R false
(4) A false, R true
๐Ÿ”ฅ3๐Ÿฅฐ3๐Ÿคฉ1
1๏ธโƒฃ #DUALBEHAVIOUROFMATTER โญ
โœ”๏ธ Matter shows dual nature:
๐Ÿ‘‰ Particle nature
๐Ÿ‘‰ Wave nature
โœ”๏ธ This concept proved that classical physics fails at atomic scale
NEET point:
โœ”๏ธ Dual behaviour mainly observed for microscopic particles (electron, proton)


2๏ธโƒฃ #PARTICLENATUREOFMATTER โญ
โœ”๏ธ Matter consists of discrete particles
โœ”๏ธ Particle nature supported by:
๐Ÿ‘‰ Photoelectric effect
๐Ÿ‘‰ Compton effect
๐Ÿ“Œ Evidence:
โœ”๏ธ Emission of electrons only when threshold frequency is reached


3๏ธโƒฃ #WAVENATUREOFMATTER โญ
โœ”๏ธ Proposed by de Broglie
โœ”๏ธ Every moving particle behaves like a wave
๐Ÿ“Œ de Broglie hypothesis:
โœ”๏ธ ฮป โˆ 1/p
๐Ÿ“Œ de Broglie wavelength:
โœ”๏ธ ฮป = h / mv
Where:
โœ”๏ธ h = Planckโ€™s constant
โœ”๏ธ m = mass
โœ”๏ธ v = velocity
NEET point:
โœ”๏ธ Wave nature important for electrons


4๏ธโƒฃ #ELECTROMAGNETICRADIATION โญ
โœ”๏ธ Energy travels as waves
โœ”๏ธ Does not require medium
๐Ÿ“Œ Examples:
โœ”๏ธ Radio waves
โœ”๏ธ Microwaves
โœ”๏ธ Infrared
โœ”๏ธ Visible light
โœ”๏ธ UV, X-rays, ฮณ-rays
๐Ÿ“Œ Relation:
โœ”๏ธ c = ฮฝฮป


5๏ธโƒฃ #PHOTOELECTRICEFFECT โšก โญ
โœ”๏ธ Emission of electrons when light falls on metal surface
๐Ÿ“Œ Key observations:
โœ”๏ธ Threshold frequency (ฮฝโ‚€) exists
โœ”๏ธ No emission below ฮฝโ‚€
โœ”๏ธ Intensity โ†‘ โ†’ number of electrons โ†‘
โœ”๏ธ Frequency โ†‘ โ†’ kinetic energy โ†‘
๐Ÿ“Œ Einsteinโ€™s photoelectric equation:
โœ”๏ธ hฮฝ = hฮฝโ‚€ + ยฝmvยฒ
NEET trap
โœ”๏ธ KE depends on frequency, NOT intensity


6๏ธโƒฃ #WAVEPARTICLEDUALITY โญ
โœ”๏ธ Light behaves as:
๐Ÿ‘‰ Wave โ†’ interference, diffraction
๐Ÿ‘‰ Particle โ†’ photoelectric effect
โœ”๏ธ Matter behaves as:
๐Ÿ‘‰ Particle โ†’ mass, momentum
๐Ÿ‘‰ Wave โ†’ de Broglie wavelength
NEET clarity:
โœ”๏ธ Dual behaviour is complementary, not simultaneous


7๏ธโƒฃ #IMPORTANCEOFDEBROGLIEWAVE โญ
โœ”๏ธ Basis of Bohrโ€™s model modification
โœ”๏ธ Explains stability of orbits
โœ”๏ธ Used in electron microscope

๐Ÿ“Œ Special cases:
โœ”๏ธ For electron (accelerated by V):
ฮป = h / โˆš(2meV)


8๏ธโƒฃ #NEETONELINERS
โœ”๏ธ Dual nature โ†’ matter + radiation
โœ”๏ธ Threshold frequency โ†’ metal dependent
โœ”๏ธ de Broglie wavelength inversely โˆ velocity
โœ”๏ธ Electron shows wave nature more clearly


9๏ธโƒฃ #FORMULASUMMARY (MUST REVISE )
โœ”๏ธ ฮป = h / mv
โœ”๏ธ c = ฮฝฮป
โœ”๏ธ E = hฮฝ
โœ”๏ธ hฮฝ = hฮฝโ‚€ + ยฝmvยฒ
โœ”๏ธ ฮป = h / โˆš(2meV)


๐Ÿ”Ÿ #REAL_SENSESUMMARY โญ
โœ”๏ธ Classical physics โŒ at atomic scale
โœ”๏ธ Quantum ideas โœ”๏ธ required
โœ”๏ธ Wave nature dominates for small particles
โœ”๏ธ Foundation of modern chemistry & physics

@Ayano1me @Neetugpoll @Neetugquiz
โค3๐Ÿฅฐ2๐Ÿ•Š2๐Ÿ’‹2
1๏ธโƒฃ #DIPOLEMOMENT
๐Ÿ“Œ Measure of polarity of a bond or molecule


2๏ธโƒฃ #DEFINITION
โœ”๏ธ Product of magnitude of charge (q) and distance (d) between centres of +ve and โˆ’ve charges
โœ”๏ธ ฮผ = q ร— d
โœ”๏ธ Vector quantity
โœ”๏ธ Direction โ†’ from negative to positive charge


3๏ธโƒฃ #UNITS
โœ”๏ธ SI unit โ†’ Coulomb metre (Cยทm)
โœ”๏ธ Practical unit โ†’ Debye (D)
๐Ÿ“Œ 1 Debye = 3.336 ร— 10โปยณโฐ Cยทm


4๏ธโƒฃ #BONDDIPOLEMOMENT
โœ”๏ธ Due to electronegativity difference
โœ”๏ธ Greater ฮ”EN โ†’ greater dipole moment
๐Ÿ“Œ Hโ€“Cl > Hโ€“Br > Hโ€“I


5๏ธโƒฃ #MOLECULARDIPOLEMOMENT
โœ”๏ธ Vector sum of all bond dipoles
โœ”๏ธ Depends on molecular shape & symmetry


6๏ธโƒฃ #EFFECTOFSHAPE
โœ”๏ธ Symmetrical molecule โ†’ ฮผ = 0
โœ”๏ธ Unsymmetrical molecule โ†’ ฮผ โ‰  0
๐Ÿ“Œ Examples:
โœ”๏ธ COโ‚‚ โ†’ ฮผ = 0 (linear)
โœ”๏ธ BFโ‚ƒ โ†’ ฮผ = 0 (trigonal planar)
โœ”๏ธ Hโ‚‚O โ†’ ฮผ โ‰  0 (bent)
โœ”๏ธ NHโ‚ƒ โ†’ ฮผ โ‰  0 (pyramidal)


7๏ธโƒฃ #APPLICATIONS
โœ”๏ธ Polarity determination
โœ”๏ธ Molecular geometry
โœ”๏ธ Ionic character
โœ”๏ธ Distinguishing cisโ€“trans isomers
๐Ÿ“Œ cis โ†’ ฮผ โ‰  0
๐Ÿ“Œ trans โ†’ ฮผ = 0


8๏ธโƒฃ #IMPORTANTNCERTPOINTS
โœ”๏ธ Lone pair increases dipole moment
โœ”๏ธ Symmetry can cancel dipole moment
โœ”๏ธ Polar bonds may give zero ฮผ


9๏ธโƒฃ #NEETTRAPS
โŒ Polar bond โ‰  polar molecule
โŒ Zero ฮผ โ‰  non-polar bonds
โŒ Shape ignored = wrong answer
HF>HCL but ch3cl>ch3F ( DM)


@Ayano1me @Neetugpoll @Neetugquiz
๐Ÿ˜2โค1๐Ÿ‘1๐Ÿ”ฅ1๐Ÿ™1
Aaj 8 bje all book module ka link
โค3๐Ÿ”ฅ3๐Ÿ‘2๐Ÿ‘Œ1
1๏ธโƒฃ #VSEPRTHEORY
๐Ÿ“Œ VSEPR = Valence Shell Electron Pair Repulsion theory
๐Ÿ“Œ Used to predict shape of molecules and ions.


2๏ธโƒฃ #BASICIDEA
โœ”๏ธ Electron pairs in valence shell repel each other
โœ”๏ธ They arrange themselves to minimise repulsion
โœ”๏ธ Shape depends on number of electron pairs around central atom


3๏ธโƒฃ #TYPESOFELECTRONPAIRS
โœ”๏ธ Bond pair (BP) โ€“ shared electrons
โœ”๏ธ Lone pair (LP) โ€“ unshared electrons
๐Ÿ“Œ Lone pair occupies more space than bond pair


4๏ธโƒฃ #ORDEROFREPULSION (VERY IMP ๐Ÿ”ฅ)
โœ”๏ธ LPโ€“LP > LPโ€“BP > BPโ€“BP
๐Ÿ“Œ This order decides distortion in shape


5๏ธโƒฃ #ELECTRONGEOMETRYVS MOLECULARGEOMETRY
โœ”๏ธ Electron geometry โ†’ arrangement of all electron pairs
โœ”๏ธ Molecular geometry โ†’ arrangement of atoms only
๐Ÿ“Œ Lone pairs affect molecular shape, not electron geometry


6๏ธโƒฃ #IDEALGEOMETRIES (NO LONE PAIR)
โœ”๏ธ 2 BP โ†’ Linear โ†’ 180ยฐ โ†’ BeClโ‚‚
โœ”๏ธ 3 BP โ†’ Trigonal planar โ†’ 120ยฐ โ†’ BFโ‚ƒ
โœ”๏ธ 4 BP โ†’ Tetrahedral โ†’ 109.5ยฐ โ†’ CHโ‚„
โœ”๏ธ 5 BP โ†’ Trigonal bipyramidal โ†’ PClโ‚…
โœ”๏ธ 6 BP โ†’ Octahedral โ†’ SFโ‚†


7๏ธโƒฃ #EFFECTOFLONEPAIR
โœ”๏ธ Lone pair reduces bond angle
โœ”๏ธ More lone pairs โ†’ more deviation from ideal shape
๐Ÿ“Œ Examples:
โœ”๏ธ CHโ‚„ โ†’ 109.5ยฐ
โœ”๏ธ NHโ‚ƒ โ†’ 107ยฐ
โœ”๏ธ Hโ‚‚O โ†’ 104.5ยฐ


8๏ธโƒฃ #SPECIALCASESTRIGONALBIPYRAMIDAL
โœ”๏ธ Axial positions โ†’ more repulsion
โœ”๏ธ Equatorial positions โ†’ less repulsion
๐Ÿ“Œ Lone pair occupies equatorial position first
๐Ÿ“Œ Example:
โœ”๏ธ SFโ‚„ โ†’ seesaw
โœ”๏ธ ClFโ‚ƒ โ†’ T-shape
โœ”๏ธ XeFโ‚‚ โ†’ linear


9๏ธโƒฃ #SPECIALCASEOFOCTAHEDRAL
โœ”๏ธ One lone pair โ†’ square pyramidal
โœ”๏ธ Two lone pairs โ†’ square planar
๐Ÿ“Œ Examples:
โœ”๏ธ BrFโ‚… โ†’ square pyramidal
โœ”๏ธ XeFโ‚„ โ†’ square planar


๐Ÿ”Ÿ #NEETIMPORTANTPOINTS ๐Ÿšจ
โœ”๏ธ Lone pair causes maximum repulsion
โœ”๏ธ Shape decided by LP + BP count
โœ”๏ธ VSEPR explains shape, not bonding strength
โœ”๏ธ Used mainly for p-block compounds


1๏ธโƒฃ1๏ธโƒฃ #LIMITATIONSOFVSEPR
โœ”๏ธ Cannot explain bond length accurately
โœ”๏ธ Not applicable for transition metals
โœ”๏ธ Fails for odd-electron molecules


1๏ธโƒฃ2๏ธโƒฃ #ONELINEREVISION
Molecular shape is decided by repulsion between electron pairs around the central atom.

@Ayano1me @Neetugpoll @Neetugquiz
๐Ÿ”ฅ2๐Ÿ˜Ž2โค1๐Ÿ’‹1
โค2๐Ÿคฉ1๐Ÿ’ฏ1๐Ÿ˜˜1
Chemistry booster series
https://t.me/+5VTfeOK6KxJkYWQ1
Old m Copyright aa gya ๐Ÿ™‚again upload krenge 3500+ video

Btw share krdo needy students ko baad m link na milegi
๐Ÿ’ฏ4โค2๐Ÿ•Š1๐Ÿ˜1
1๏ธโƒฃ #MOLECULARORBITALTHEORY
๐Ÿ“Œ Molecular Orbital Theory (MOT) explains bonding, bond order and magnetic nature of molecules.
๐Ÿ“Œ Proposed by Hund and Mulliken.


2๏ธโƒฃ #BASICIDEA
โœ”๏ธ Atomic orbitals of bonded atoms combine to form molecular orbitals
โœ”๏ธ Molecular orbitals belong to the entire molecule
โœ”๏ธ Number of MOs formed = number of AOs combined


3๏ธโƒฃ #CONDITIONSFORCOMBINATION
โœ”๏ธ Comparable energy of AOs
โœ”๏ธ Proper orientation
โœ”๏ธ Significant overlap


4๏ธโƒฃ #TYPESOFMOLECULARORBITALS
โœ”๏ธ Bonding MO
โœ”๏ธ Antibonding MO
โœ”๏ธ Non-bonding MO (rare in diatomic molecules)


5๏ธโƒฃ #BONDINGMO
โœ”๏ธ Formed by constructive overlap
โœ”๏ธ Lower energy than AOs
โœ”๏ธ Increases stability
๐Ÿ“Œ Denoted by: ฯƒ, ฯ€


6๏ธโƒฃ #ANTIBONDINGMO
โœ”๏ธ Formed by destructive overlap
โœ”๏ธ Higher energy
โœ”๏ธ Decreases stability
๐Ÿ“Œ Denoted by: ฯƒ*, ฯ€*


7๏ธโƒฃ #ELECTRONFILLINGRULES
โœ”๏ธ Aufbau principle
โœ”๏ธ Pauli exclusion principle
โœ”๏ธ Hundโ€™s rule of maximum multiplicity


8๏ธโƒฃ #ENERGYORDEROFDIATOMICMOLECULES โญ
๐Ÿ“Œ For Bโ‚‚, Cโ‚‚, Nโ‚‚:
ฯƒ1s < ฯƒ1s < ฯƒ2s < ฯƒ2s < ฯ€2p < ฯƒ2p < ฯ€2p < ฯƒ2p
๐Ÿ“Œ For Oโ‚‚, Fโ‚‚, Neโ‚‚:
ฯƒ1s < ฯƒ1s < ฯƒ2s < ฯƒ2s < ฯƒ2p < ฯ€2p < ฯ€2p < ฯƒ2p


9๏ธโƒฃ #BONORDER (VERY IMP )
๐Ÿ“Œ Formula:
Bond order = (Nb โˆ’ Na) / 2
โœ”๏ธ Nb = bonding electrons
โœ”๏ธ Na = antibonding electrons
๐Ÿ“Œ Interpretation:
โœ”๏ธ Higher bond order โ†’ stronger bond
โœ”๏ธ Bond order = 0 โ†’ molecule does not exist


๐Ÿ”Ÿ #MAGNETICNATURE
โœ”๏ธ Unpaired electrons โ†’ paramagnetic
โœ”๏ธ All electrons paired โ†’ diamagnetic
๐Ÿ“Œ Example:
โœ”๏ธ Oโ‚‚ โ†’ paramagnetic
โœ”๏ธ Nโ‚‚ โ†’ diamagnetic


1๏ธโƒฃ1๏ธโƒฃ #IMPORTANTEXAMPLES (NEET ๐Ÿ”ฅ)
โœ”๏ธ Hโ‚‚ โ†’ bond order = 1
โœ”๏ธ Heโ‚‚ โ†’ bond order = 0 (does not exist)
โœ”๏ธ Oโ‚‚โบ โ†’ bond order increases
โœ”๏ธ Oโ‚‚โป โ†’ bond order decreases


1๏ธโƒฃ2๏ธโƒฃ #LIMITATIONSOFMOT
โœ”๏ธ Complex for polyatomic molecules
โœ”๏ธ Does not explain shape clearly


1๏ธโƒฃ3๏ธโƒฃ #NEETIMPORTANTPOINTS
โœ”๏ธ MOT explains paramagnetism of Oโ‚‚
โœ”๏ธ Energy order changes after Nโ‚‚
โœ”๏ธ Bond order decides stability


1๏ธโƒฃ4๏ธโƒฃ #ONELINEREVISION
Molecular Orbital Theory explains bonding by delocalised molecular orbitals and predicts bond order and magnetic nature

@Ayano1me @Neetugpoll @Neetugquiz
๐Ÿฅฐ2โค1๐Ÿ’ฏ1
1๏ธโƒฃ #VALENCEBONDTHEORY
๐Ÿ“Œ Valence Bond Theory (VBT) explains formation of covalent bonds by overlap of atomic orbitals.
๐Ÿ“Œ Proposed by Heitler and London.


2๏ธโƒฃ #BASICIDEA
โœ”๏ธ Atoms bond to achieve stable electronic configuration
โœ”๏ธ Half-filled atomic orbitals overlap
โœ”๏ธ Electrons pair with opposite spins
๐Ÿ“Œ Greater overlap โ†’ stronger bond


3๏ธโƒฃ #CONDITIONSFOROVERLAP
โœ”๏ธ Half-filled orbitals
โœ”๏ธ Comparable energy of orbitals
โœ”๏ธ Proper orientation


4๏ธโƒฃ #TYPESOFOBOND
โœ”๏ธ Sigma (ฯƒ) bond
โœ”๏ธ Pi (ฯ€) bond


5๏ธโƒฃ #SIGMABOND
โœ”๏ธ Formed by head-on overlap
โœ”๏ธ Stronger than ฯ€ bond
โœ”๏ธ Electron density along internuclear axis
๐Ÿ“Œ Overlap types:
โœ”๏ธ sโ€“s
โœ”๏ธ sโ€“p
โœ”๏ธ pโ€“p


6๏ธโƒฃ #PIBOND
โœ”๏ธ Formed by sidewise overlap
โœ”๏ธ Weaker than ฯƒ bond
โœ”๏ธ Electron density above & below axis
๐Ÿ“Œ Formed by pโ€“p overlap only


7๏ธโƒฃ #HYBRIDISATION
๐Ÿ“Œ Mixing of atomic orbitals of similar energy to form hybrid orbitals.
โœ”๏ธ Number of hybrid orbitals = number of AOs mixed


8๏ธโƒฃ #TYPESOFHYBRIDISATION
โœ”๏ธ sp โ†’ linear โ†’ 180ยฐ โ†’ BeClโ‚‚
โœ”๏ธ spยฒ โ†’ trigonal planar โ†’ 120ยฐ โ†’ BFโ‚ƒ
โœ”๏ธ spยณ โ†’ tetrahedral โ†’ 109.5ยฐ โ†’ CHโ‚„
โœ”๏ธ dspยฒ โ†’ square planar โ†’ [Ni(CN)โ‚„]ยฒโป
โœ”๏ธ dยฒspยณ โ†’ octahedral โ†’ [Co(NHโ‚ƒ)โ‚†]ยณโบ


9๏ธโƒฃ #VALENCEBONDTHEORYINCOORDINATIONCOMPOUNDS
โœ”๏ธ Central metal provides empty orbitals
โœ”๏ธ Ligands donate lone pair
โœ”๏ธ Coordinate bond formed by overlap


๐Ÿ”Ÿ #MAGNETICNATURE
โœ”๏ธ Unpaired electrons โ†’ paramagnetic
โœ”๏ธ Paired electrons โ†’ diamagnetic
๐Ÿ“Œ Example:
โœ”๏ธ [Ni(CN)โ‚„]ยฒโป โ†’ diamagnetic
โœ”๏ธ [NiClโ‚„]ยฒโป โ†’ paramagnetic


1๏ธโƒฃ1๏ธโƒฃ #LIMITATIONSOFVBT
โœ”๏ธ Cannot explain colour of compounds
โœ”๏ธ Cannot explain strong vs weak ligands clearly
โœ”๏ธ No quantitative explanation of spectra


1๏ธโƒฃ2๏ธโƒฃ #NEETIMPORTANTPOINTS
โœ”๏ธ ฯƒ bond is stronger than ฯ€ bond
โœ”๏ธ Multiple bonds = 1 ฯƒ + remaining ฯ€
โœ”๏ธ Hybridisation explains geometry


1๏ธโƒฃ3๏ธโƒฃ #ONELINEREVISION
Valence Bond Theory explains bonding by orbital overlap and predicts bond type, strength and geometry.

@Ayano1me @Neetugpoll @Neetugquiz
๐Ÿ”ฅ2๐Ÿ†1๐Ÿ™ˆ1