Chemistry 1 Resources
Proton
Neutron
Electron
H --- 1 proton
He --- 2 proton, 2 neutron
Li --- 3 proton, 4 neutron
Be --- 4 proton, 5 neutron
B --- 5 proton, 6 neutron
C --- 6 proton, 6 neutron
N --- 7 proton, 7 neutron
O --- 8 proton, 8 neutron
F --- 9 proton, 9 neutron
Ne --- 10 proton, 10 neutron
Na --- 11 proton, 11 neutron
Mg --- 12 proton, 12 neutron
Al --- 13 proton, 14 neutron
Hydrogen ion (H+) = Proton
Ion
ionization, excitation
absorption of photon - excitation of electron
Isotope
Hydrogen: Protium, Deuterium, Tritium
Alpha particle = Helium ion
Beta plus particle = Positron. Positively charged electron.
P (proton) --> N (neutron) + weak boson --> N + positron + neutrino.
Positron emission = 1P --> 1N + positron + neutrino.
When an element has more protons than neutrons, a proton will split into a positron and a neutron. The positron is then emitted as beta plus radiation.
Beta minus particle = Electron.
N (neutron) --> P (proton) + weak boson --> P + electron + anti-neutrino.
Beta emission = 1N --> 1P + electron + anti-neutrino.
When an element has more neutron than protons, a neutron will split into a proton and an electron. The electron is then emitted as beta minus radiation.
X ray particle = Photon with higher frequency than ultraviolet.
X ray emission = relaxation of an electron + photon. An electron will emit a photon (X ray) spontaneously with relaxation.
Gamma ray particle = Photon with the highest frequency.
Gamma ray emission = de-excitation of proton + photon.
Neutrino emission. When an element is poor in neutron, the nucleus will capture an electron, a proton is changed to a neutron, and one type of neutrino (electron neutrino) is released.
Electron capture = 1P + electron --> 1N + neutrino.
Neutron emission = 1N loss + 1N emission
1 s
2 s p
3 s p d
4 s p d f
5 s p d f g
6 s p d f g h
7 s p d f g h i
s - 1 orbital
p - 3 orbitals
d - 5 orbitals
f - 7 orbitals
Each orbital can accommodate up to 2 electrons.
s - 1 orbital - 2 electrons
p - 3 orbitals - 6 electrons
d - 5 orbitals - 10 electrons
f - 7 orbitals - 14 electrons
1 s
2 electrons = (1x1) x2 = 2
2 s p
2 + 6 electrons = (2x2) x2 = 8
3 s p d
2 + 6 + 10 electrons = (3x3) x2 = 18
4 s p d f
2 + 6 + 10 + 14 electrons = (4x4) x2 = 32
5 s p d f g
6 s p d f g h
7 s p d f g h i
1s H, He
2s Li, Be
2p B, C
2p N, O
2p F, Ne
Li
Be
B
C
N
O
F
Ne
3s Na, Mg
3p Al, Si
3p P, S
3p Cl, Ar
4s K, Ca
3d Sc, Ti
3d V, Cr
3d Mn, Fe
3d Co, Ni
3d Cu, Zn
4p Ga, Ge
4p As, Se
4p Br, Kr
5s Rb, Sr
4d Y, Zr
4d Nb, Mo
4d Tc, Ru
4d Rh, Pd
4d Ag, Cd
5p In, Sn
5p Sb, Te
5p I, Xe
6s Cs, Ba
4f
4f
4f
4f
4f
4f
4f
5d
5d
5d
5d
5d
6p
6p
6p
7s
5f
5f
5f
5f
5f
5f
5f
6d
6d
6d
6d
6d
Single covalent bond ( = 1 sigma bond)
Double covalent bond ( = 1 sigma bond + 1 pi bond)
Triple covalent bond ( = 1 sigma bond + 2 pi bonds)
Two double covalent bonds ( = 2 sigma bonds + 2 pi bonds)
SP orbital hybridization
S orbital and P orbital sometimes merges and becomes indistinctive/indistinguishable.
SP1 Linear hybridization
When the outer electrons are attracted by two H atoms from two directions, a 2S orbital and one 2P orbital will hybridize and create a new "SP orbital". The SP orbital contributes to the creation of two directed sigma bonds.
Attracted in 2 directions...
2s and 2px disappear, and...
then re-appear as an sp1 orbit.
2py and 2pz are left anaffected.
One SP hybrid orbital has 2 arms. (linear)
Example:
Carbon with SP1 hybridization
Nitrogen with SP1 hybridization
Oxygen with SP1 hybridization???
(This won't exist)
SP2 Triangular hybridization
When the outer electrons are attracted by three H atoms from three directions, 2S and two of 2P orbitals will create three new identical SP2 orbitals and contribute to the creation of 3-directed sigma bonds.
Attracted in 3 directions...
2s, 2px, 2py disappear, and...
then, re-appear as an sp2 orbit.
2pz is left unaffected.
One SP2 hybrid orbital has 3 arms. (triangular)
Example:
Carbon with SP2 hybridization
Nitrogen with SP2 hybridization
Oxygen with SP2 hybridization
SP3 Tetrahedral hybridization
When the outer electrons are attracted by four H atoms from four directions, 2S and all three 2P orbitals will create four new identical SP3 orbitals and contribute to the creation of 4 sigma bonds.
Attracted in 4 directions...
2s, 2px, 2py, 2pz disappear, and...
then, re-appear as an sp3 orbit.
One SP3 hybrid orbital has 4 arms. (tetrahedron)
No 2p orbitals are left unaffected.
Example:
Carbon with SP3 hybridization
Nitrogen with SP3 hybridization
Oxygen with SP3 hybridization
Ex1. Dihydrogen (HH)
No hybrid orbitals is created. One sigma bond (one single covalent bond) between H and H is observed.
H-H
H:H
Single covalent bond ( = 1 sigma bond)
Ex2. O2
1. Non-hybridization
2. sp2 hybridization. An sp2 trigonal hybridization is created with one 2p orbital left alone. One double covalent bond (one sigma bond and one pi bond) is seen between O and O.
O=O
O::O
Double covalent bond ( = 1 sigma bond + 1 pi bond)
Ex3. CO2
An sp linear hybridization of C is created. Also an sp2 trigonal hybridization of O is created. Two double covalent bonds (2 sigma bonds and 2 pi bonds) are seen between C and O.
O=C=O
O::C::O
Double covalent bond ( = 1 sigma bond + 1 pi bond)
Ex 4. NH3
An sp3 hybridization of N is created. The sp3 hybrid orbital has 3 arms. There are 3 sigma bonds (3 single covalent bond) seen between N and H.
N without hybridization
When N is attracted in 3 directions, tetrapod is created...
2s, 2px, 2py, 2px disappear, and...
N with sp3 hybridization created.
cf. SP2 hybridization of Nitrogen
H-N=N-N
H:N::N:H
Double covalent bond ( = 1 sigma bond + 1 pi bond)
cf. SP1 hybridization of Nitrogen
N≡N
N:::N
Triple covalent bond ( = 1 sigma bond + 2 pi bonds)
Ex5. H2O
Not well known. 2 possibilities. Theory 1 more likely.
1: An sp3 hybridization of O is created. The sp3 hybrid orbital has 3 arms and two of these arms are involved in sigma bonds between O and H.
2: No hybridization is involved. Two of 3 unhybridized 2px 2py 2pz orbitals create 2 sigma bonds (two single covalent bond) between O and H.
O without hybridization
When O is attracted in 2 directions, tetrapod is created...
2s, 2px, 2py, 2pz disappear, and...
O with an sp3 orbit created.
H-O-H
H:O:H
Ex6. Methane (CHHHH)
An sp3 hybridization of C is created. The sp3 hybrid orbital creates 4 arms. There are 4 sigma bonds (four single covalent bonds) between C and H.
Ex7. Ethane (HHHCCHHH)
An sp3 hybridization of C is created, One sigma bond (one single covalent bond) is seen between C and C.
C-C
C:C
Single covalent bond ( = 1 sigma bond)
Ex8. Ethylene (HHCCHH) = Ethene
An sp2 trigonal hybridization of C is created. The sp2 hybrid orbital creates 3 arms. One double covalent bond (one sigma bond and one pi bond) is seen between C and C.
C=C
C::C
Double covalent bond ( = 1 sigma bond + 1 pi bond)
Ex9. Acetylene (HCCH)
An sp linear hybridization of C is created. The sp hybrid orbital creates 2 arms. One triple covalent bond (one sigma bond and two pi bonds) is seen between C and C.
H-C≡C-HH:C:::C:H
Triple covalent bond ( = 1 sigma bond + 2 pi bonds)
Ex10. Benzene
An sp2 trigonal hybridation of C is created. The sp2 hybrid orbital has 3 arms. Each pz orbital creates pi bonds among C.
C with sp2 hybridization
Benzene ring (conjugated)
(© 2015 Pearson Education, Inc.)
(Chemistry Chapter 9 Molecular Geometry and Bonding Theories)
(https://byjus.com/jee/hybridization-of-benzene/)
Beryllium sp linear hybridization
BH3 sp2 trigonal hybridization
The sp linear hybridization is normally not encountered in oxygen compounds.
Oxidation: a loss of electrons (or a loss of hydrogen atom)
Reduction: a gain of electrons (or a gain of hydrogen atom)
Acid: proton (hydrogen ion) donor, molecule accepting electron pair, will produce H3O+ in water
Base: proton (hydrogen ion) acceptor, molecule giving electron pair, will produce OH- in water
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