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Chemical Bonding Copyright Sautter 2003
The next slide is a quick promo for my books  after which the presentation will begin Thanks for your patience! Walt S. [e...
Books available at: www. wsautter .com www.smashwords.com www.amazon.com www.bibliotastic.com www.goodreads.com Walt’s Boo...
Cl H CHEMICAL BONDS BONDS HOLD ATOMS TOGETHER TO FORM MOLECULES
TYPES OF CHEMICAL BONDS <ul><li>(1) IONIC BONDS -  ELECTRONS AS TRANSFERRED FROM METALS TO NONMETALS (IONIC SALTS FOR EXAM...
WHY DO BONDS BETWEEN ATOMS FORM ? <ul><li>WHEN BONDS FORM THE STABILITY OF THE COMBINED ATOMS INCREASES AS COMPARED TO THA...
+9 +19 2e 1e 8e 18e K F K+ F- 7e 2e 8e IONIC BOND FORMATION - ELECTRON TRANSFER BETWEEN METALS & NONMETALS =  a valence el...
REPRESENTING ATOMS AND MOLECULES  USING ELECTRON DOT FORMULAE (LEWIS DOT REPRESENTATIONS) <ul><li>LEWIS DOT FORMULAE USE T...
ELECTRON DOT REPRESENTATIONS  FOR SOME COMMON ATOMS (LEWIS DOT NOTATIONS) H Li Be B C N O F Ne . . . . . . . . . . . . . ....
COMMON PROPERTIES AND CHARACTERISTICS OF COVALENT BONDS <ul><li>COVALENT BONDS MAY BE SINGLE, DOUBLE OR TRIPLE BONDS </li>...
COVALENT BONDING (ELECTRON SHARING – SINGLE BOND) +9 +9 2e 7e F F 7e 2e F 2 =  a valence electron 6e 6e F F : : : . . . . ...
COVALENT BONDING (ELECTRON SHARING – DOUBLE BOND) +8 +8 2e 6e O O 6e 2e O 2 =  a valence electron 4e 4e O O . . . . : : : ...
COVALENT BONDING (ELECTRON SHARING – TRIPLE BOND) +7 +7 2e 5e N N 5e 2e N 2 =  a valence electron 2e 2e N N : : : : : BOTH...
ELECTRON DOT REPRESENTATIONS OF POLYATOMIC MOLECULES AND IONS WRITING THE DOT FORMULA FOR METHANE - CH 4 STEP I – DETERMIN...
WRITING THE DOT FORMULA FOR METHANE CH 4  C H H H H STEP III -PLACE TWO DOTS (ELECTRONS)  BETWEEN EACH BONDED PAIR OF ATOM...
WRITING THE ELECTRON STRUCTURE FOR  MONOCHLOROETHENE - C 2 H 3 Cl  2 C = 2 x 4 = 8 e 3 H = 3 x 1 = 3 e 1 Cl = 1 x 7 = 7 e ...
WRITING ELECTRON DOT REPRESENTATIONS FOR POLYATOMIC IONS CONTAINING RESONANCE  STRUCTURES (CARBONATE ION -  CO 3 -2  ) 1 C...
RESONANCE STRUCTURES OCCUR WHEN A DOUBLE OR TRIPLE BOND MAY EQUALLY WELL BE PLACED AT MORE THAN ONE BONDING SITE FOR EXAMP...
WHEN RESONANCE OCCURS THE DOUBLE BOND  IS SAID TO BE DELOCALIZED WHICH MEANS  THAT IT MOVES CONTINUALLY FROM ONE BONDING S...
COMMON PROPERTIES AND CHARACTERISTICS OF COVALENT BONDS (CONT’D) <ul><li>COVALENT BONDS MAY BE POLAR OR NONPOLAR </li></ul...
COMMON PROPERTIES AND CHARACTERISTICS OF COVALENT BONDS (CONT’D) <ul><li>THE DEGREE OF BOND POLARITY DEPENDS ON HOW WELL O...
COMMON PROPERTIES AND CHARACTERISTICS OF COVALENT BONDS (CONT’D) <ul><li>THE LARGEST POSSIBLE DIFFERENCE IN ELECTRONEGATIV...
KINDS OF CHEMICAL BONDS <ul><li>IONIC BONDING </li></ul><ul><li>   EN = (4.0 – 0.70) = 3.3  </li></ul><ul><li>POLAR COVAL...
BOND FORMATION AND HYBRIDIZATION <ul><li>ATOMS GENERALLY FORM AS MANY BONDS AS IS POSSIBLE. OFTEN THE BONDING CAPACITY OF ...
BOND FORMATION AND HYBRIDIZATION (CONT’D) <ul><li>RULES GOVERNING ORBITAL HYBRIDIZATION </li></ul><ul><li>(1) THE NUMBER O...
HYBRIDIZATION AND PERIODIC TRENDS <ul><li>TRENDS IN BONDING BETWEEN ATOMS OCCUR IN SIMILAR FASHION AMONG MEMBERS OF THE SA...
UNHYBRIDIZED LITHIUM (BEFORE REACTING) 3P 2S 1S Li LITHIUM LITHIUM WITH NO HYBRIDIZATION  (CAPABLE OF FORMING ONE BOND) NO...
UNHYBRIDIZED BERYLLIUM (BEFORE REACTING) 3P 2S 1S Be BERYLLIUM SP HYBRID ORBITALS BERYLLIUM IN HYBRIDIZED STATE  (CAPABLE ...
UNHYBRIDIZED BORON (BEFORE REACTING) 3P 2S   1S B BORON SP 2  HYBRID ORBITALS BORON IN HYBRIDIZED STATE  (CAPABLE OF FORMI...
UNHYBRIDIZED CARBON (BEFORE REACTING) 3P 2S   1S C CARBON SP 3  HYBRID ORBITALS CARBON IN HYBRIDIZED STATE  (CAPABLE OF FO...
UNHYBRIDIZED NITROGEN (BEFORE REACTING) 3P 2S 1S N NITROGEN SP 3  HYBRID ORBITALS NITROGEN IN HYBRIDIZED STATE  (CAPABLE O...
UNHYBRIDIZED OXYGEN (BEFORE REACTING) 3P 2S   1S O OXYGEN SP 3  HYBRID ORBITALS OXYGEN IN HYBRIDIZED STATE  (CAPABLE OF FO...
UNHYBRIDIZED CARBON (BEFORE REACTING) 3P 2S 1S F FLOURINE SP 3  HYBRID ORBITALS FLOURINE IN HYBRIDIZED STATE  (CAPABLE OF ...
N . . . . . H . . H H . H + AMMONIA NH 3 HYDROGEN ION WITH NO ELECTRONS COORDINATE COVALENT BOND FORMATION H + AMMONIUM IO...
THE END
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Chemical Bonding

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Explains chemical bonding
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Transcript of "Chemical Bonding"

  1. 1. Chemical Bonding Copyright Sautter 2003
  2. 2. The next slide is a quick promo for my books after which the presentation will begin Thanks for your patience! Walt S. [email_address] More stuff at: www.wsautter.com
  3. 3. Books available at: www. wsautter .com www.smashwords.com www.amazon.com www.bibliotastic.com www.goodreads.com Walt’s Books for Free!
  4. 4. Cl H CHEMICAL BONDS BONDS HOLD ATOMS TOGETHER TO FORM MOLECULES
  5. 5. TYPES OF CHEMICAL BONDS <ul><li>(1) IONIC BONDS - ELECTRONS AS TRANSFERRED FROM METALS TO NONMETALS (IONIC SALTS FOR EXAMPLE NaCl, CaCl 2 ) </li></ul><ul><li>(2) COVALENT BONDS – ELECTRONS ARE SHARED BETWEEN NONMETALS (DIATOMIC MOLECULES FOR EXAMPLE THE HALOGENS, F 2 , Cl 2 , etc.) </li></ul><ul><li>(3) COORDINATE COVALENT BONDS – A BONDING PAIR OF ELECTRONS IS CONTRIBUTED BY ONLY ONE ATOM IN THE BOND (FOR EXAMPLE AMMONIUM ION, NH 4 + , HYDRONIUM ION, H 3 O + ) </li></ul>
  6. 6. WHY DO BONDS BETWEEN ATOMS FORM ? <ul><li>WHEN BONDS FORM THE STABILITY OF THE COMBINED ATOMS INCREASES AS COMPARED TO THAT OF THE INDIVIDUAL ATOMS. GENERALLY CHEMICAL STABILITY IS RELATED TO THE ABILITY OF ATOMS TO ATTAIN THE ELECTRON CONFIGURATION OF AN INERT GAS. FOR MANY ATOMS THIS MEANS ACQUIRING EIGHT ELECTRONS IN THE OUTER SHELL . THIS IS CALLED AN “ OCTET ” STRUCTURE. </li></ul><ul><li>THE EXCEPTATIONS ARE SMALLER ATOMS (LIKE HYDROGEN, LITHIUM, BERYLLIUM, ETC.) THESE ATTEMPT TO ACQUIRE TWO ELECTRONS LIKE HELIUM. </li></ul><ul><li>RECALL THE TERM “ ISOELECTRONIC ”. ATOMS ATTEMPT TO BECOME ISOELECTRONIC WITH THE NEAREST INERT GAS. </li></ul>
  7. 7. +9 +19 2e 1e 8e 18e K F K+ F- 7e 2e 8e IONIC BOND FORMATION - ELECTRON TRANSFER BETWEEN METALS & NONMETALS = a valence electron K F ISOELECTRONIC WITH Ar ISOELECTONIC WITH Ne
  8. 8. REPRESENTING ATOMS AND MOLECULES USING ELECTRON DOT FORMULAE (LEWIS DOT REPRESENTATIONS) <ul><li>LEWIS DOT FORMULAE USE THE ATOMIC SYMBOL TO REPRESENT THE “KERNEL” OF THE ATOM THAT IS THE NUCLEUS AND ALL INNER ENERGY LEVEL ELECTRONS. DOTS ARE THEN USED TO REPRESENT EACH OUTER ENERGY LEVEL ELECTRON (VALENCE ELECTRONS) </li></ul><ul><li>THE PAIRING OF THESE ELECTRON “DOTS” APPROXIMATES THE PAIRINGS OF ELECTRONS IN ATOMIC AND MOLECULAR (BONDING) ORBITALS OF THE ATOM OR MOLECULE. </li></ul>
  9. 9. ELECTRON DOT REPRESENTATIONS FOR SOME COMMON ATOMS (LEWIS DOT NOTATIONS) H Li Be B C N O F Ne . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
  10. 10. COMMON PROPERTIES AND CHARACTERISTICS OF COVALENT BONDS <ul><li>COVALENT BONDS MAY BE SINGLE, DOUBLE OR TRIPLE BONDS </li></ul><ul><li>(1) SINGLE BOND – ONE PAIR OF BONDING ELECTRONS JOINS TWO ATOMS TOGETHER </li></ul><ul><li>(2) DOUBLE BOND – TWO PAIRS OF BONDING ELECTRONS JOIN TWO ATOMS TOGETHER (OCCURS PRIMARILY WITH CARBON, OXYGEN, NITROGEN AND SULFUR) </li></ul><ul><li>(3) TRIPLE BOND – THREE PAIRS OF BONDING ELECTRONS JOIN TWO ATOMS TOGETHER (OCCURS PRIMARILY WITH CARBON AND NITROGEN) </li></ul>
  11. 11. COVALENT BONDING (ELECTRON SHARING – SINGLE BOND) +9 +9 2e 7e F F 7e 2e F 2 = a valence electron 6e 6e F F : : : . . . . . . . . BOTH ISOELECTRONIC WITH Ne
  12. 12. COVALENT BONDING (ELECTRON SHARING – DOUBLE BOND) +8 +8 2e 6e O O 6e 2e O 2 = a valence electron 4e 4e O O . . . . : : : : BOTH ISOELECTRONIC WITH Ne
  13. 13. COVALENT BONDING (ELECTRON SHARING – TRIPLE BOND) +7 +7 2e 5e N N 5e 2e N 2 = a valence electron 2e 2e N N : : : : : BOTH ISOELECTRONIC WITH Ne
  14. 14. ELECTRON DOT REPRESENTATIONS OF POLYATOMIC MOLECULES AND IONS WRITING THE DOT FORMULA FOR METHANE - CH 4 STEP I – DETERMINE THE TOTAL NUMBER OF VALENCE ELECTRONS FOR ALL ATOMS. CARBON (C) HAS 4 VALENCE ELECTRONS HYDROGEN (H) ATOMS HAVE 1 VALENCE ELECTRON FOR EACH OF THE FOUR ATOMS (4 x 1 = 4) THE TOTAL NUMBER OF VALENCE ELECTRONS = 8 STEP II-SELECT THE CENTRAL ATOM (THE ONE THAT CAN FORM THE GREATEST NUMBER OF BONDS) AND PLACE THE OTHER ATOMS SYMMETRICALLY AROUND IT.
  15. 15. WRITING THE DOT FORMULA FOR METHANE CH 4 C H H H H STEP III -PLACE TWO DOTS (ELECTRONS) BETWEEN EACH BONDED PAIR OF ATOMS. STEP IV -FILL IN OCTET STRUCTURES FOR ANY REMAINING ATOMS UNTIL ALL THE ELECTRONS ARE USED.*(HYDROGEN, BERYLLIUM & BORON ARE COMMON EXCEPTATIONS TO THE OCTET RULE) OCTET (8) FOR CARBON HYDROGEN REQUIRES ONLY 2 ELECTRONS
  16. 16. WRITING THE ELECTRON STRUCTURE FOR MONOCHLOROETHENE - C 2 H 3 Cl 2 C = 2 x 4 = 8 e 3 H = 3 x 1 = 3 e 1 Cl = 1 x 7 = 7 e TOTAL VALENCE ELECTRONS =18 C C H H H Cl 8 ELECTRONS REMAIN COMPLETE OCTET FOR CHLORINE 2 ELECTRONS STILL REMAIN PLACE THEM TO COMPLETE THE OCTETS FOR BOTH CARBONS OCTETS COMPLETE DOUBLE BOND
  17. 17. WRITING ELECTRON DOT REPRESENTATIONS FOR POLYATOMIC IONS CONTAINING RESONANCE STRUCTURES (CARBONATE ION - CO 3 -2 ) 1 C = 1 x4 = 4 e 3 O = 3 x 6 = 18 e -2 CHARGE = 2 e TOTAL VALENCE ELECTRONS = 24 C O O O 18 ELECTRONS REMAIN COMPLETE THE OCTETS ALL ELECTRONS ARE USED BUT AN OCTET FOR CARBON MUST BE CREATED -2 RESONANCE BOND
  18. 18. RESONANCE STRUCTURES OCCUR WHEN A DOUBLE OR TRIPLE BOND MAY EQUALLY WELL BE PLACED AT MORE THAN ONE BONDING SITE FOR EXAMPLE IN THE CARBONATE ION PREVIOUSLY SHOWN, THE DOUBLE BOND COULD HAVE BEEN PLACE BETWEEN ANY OF THE THREE CARBON – OXYGEN BOND SITES. C O O O -2 IT COULD HAVE BEEN PLACED HERE OR HERE
  19. 19. WHEN RESONANCE OCCURS THE DOUBLE BOND IS SAID TO BE DELOCALIZED WHICH MEANS THAT IT MOVES CONTINUALLY FROM ONE BONDING SITE TO THE NEXT. C O O O -2 C O O O -2 C O O O -2
  20. 20. COMMON PROPERTIES AND CHARACTERISTICS OF COVALENT BONDS (CONT’D) <ul><li>COVALENT BONDS MAY BE POLAR OR NONPOLAR </li></ul><ul><li>(1) POLAR BONDS OCCUR WHEN SHARED ELECTRON PAIRS ARE SHIFTED AWAY FROM ONE OF THE BONDED ATOMS AND TOWARDS THE OTHER. ONE END OF THE BOND THEREFORE IS MADE MORE NEGATIVE AND THE OTHER END OF THE BOND IS LEFT MORE POSITIVE. THE GREATER THE ELECTRON SHIFT, THE MORE POLAR THE BOND BECOMES. </li></ul><ul><li>(2) NONPOLAR BONDS OCCUR WHEN ELECTRON PAIRS ARE SHARED EQUALLY AND THE BOND PAIR IS CENTRALLY LOCATED BETWEEN THE ATOMS. THIS BOND HAS NO POSITIVE OR NEGATIVE END. </li></ul>
  21. 21. COMMON PROPERTIES AND CHARACTERISTICS OF COVALENT BONDS (CONT’D) <ul><li>THE DEGREE OF BOND POLARITY DEPENDS ON HOW WELL ONE ATOM ATTRACTS ELECTRONS AS COMPARED TO THE OTHER BONDED ATOM. </li></ul><ul><li>MORE NONMETALLIC ATOMS (HIGH ELECTRONEGATIVITIES) ATTRACT ELECTRONS THE BEST WHILE METALLIC ATOMS (LOW ELECTRONEGATIVITIES) ATTRACT ELECTRONS MOST POORLY. </li></ul><ul><li>WHEN BOTH BONDED ATOMS ARE NONMETALLIC THEIR ELECTRONEGATIVITY VALUES ARE COMPARED TO DETERMINE THE DEGREE OF BOND POLARITY. </li></ul>
  22. 22. COMMON PROPERTIES AND CHARACTERISTICS OF COVALENT BONDS (CONT’D) <ul><li>THE LARGEST POSSIBLE DIFFERENCE IN ELECTRONEGATIVITIES BETWEEN BONDED ATOMS IS THAT FOR A CESIUM FLOURINE BOND (  EN = 3.3) THIS REPRESENTS THE MOST IONIC POSSIBLE BOND. </li></ul><ul><li>THE SMALLEST POSSIBLE DIFFERENCE IN ELECTRONEGATIVITIES BETWEEN BONDED ATOMS OCCURS IN ALL DIATOMIC MOLECULES. SINCE EACH AOM HAS THE SAME ELECTRONEGATIVITY, THE DIFFERENCE IS ZERO (  EN = 0). THIS REPRESENTS A COMPLETELY NONPOLAR BOND. </li></ul><ul><li>ELECTRONEGATIVITY DIFFERENCES BETWEEN THESE EXTREMES (3.3 AND 0) INDICATE THE RELATIVE POLARITY OF A BOND </li></ul>
  23. 23. KINDS OF CHEMICAL BONDS <ul><li>IONIC BONDING </li></ul><ul><li> EN = (4.0 – 0.70) = 3.3 </li></ul><ul><li>POLAR COVALENT </li></ul><ul><li>BONDING </li></ul><ul><li> EN = (3.0 – 2.5) = 0.5 </li></ul><ul><li>NON POLAR </li></ul><ul><li>COVALENT BONDING </li></ul><ul><li> EN = (3.0 –3.0) = 0 </li></ul>Cs F + - C Cl -  +  Cl Cl - -
  24. 24. BOND FORMATION AND HYBRIDIZATION <ul><li>ATOMS GENERALLY FORM AS MANY BONDS AS IS POSSIBLE. OFTEN THE BONDING CAPACITY OF AN ATOM CAN BE INCREASED BY A PROCESS KNOWN AS HYBRIDIZATION. </li></ul><ul><li>IN THIS PROCESS, ORBITALS THAT ARE CLOSE TO EACHOTHER (IN TERMS OF ENERGY) MERGE TOGETHER FORMING NEW ORBITALS CALLED HYBRIDS. THE FORMATION OF THESE NEW HYBRIDS ALLOW PREVIOUSLY PAIRED ELECTRONS TO SEPARATE AN MOVE INTO NEW ORBITALS THEREBY ALLOWING FOR MORE BONDS TO BE FORMED. </li></ul><ul><li>ORBITALS COMMONLY ENGAGING IN THIS PROCESS ARE S AND P ORBITALS AT THE SAME ENERGY LEVEL. EVEN S, P AND D ORBITALS CAN HYBRIDIZE. </li></ul>
  25. 25. BOND FORMATION AND HYBRIDIZATION (CONT’D) <ul><li>RULES GOVERNING ORBITAL HYBRIDIZATION </li></ul><ul><li>(1) THE NUMBER OF HYBRID ORBITALS THAT ARE FORMED EQUAL THE NUMBER OF ATOMIC ORBITALS USED IN THE HYBRIDIZATION. </li></ul><ul><li>(2) ALL THE NEWLY FORMED HYBRID ORBITALS ARE OF EQUAL ENERGY. </li></ul><ul><li>(3) LIKE ATOMIC ORBITALS, A MAXIMUM OF TWO ELECTRONS CAN BE PRESENT. </li></ul><ul><li>(4) AN ELECTRON PAIR PRESENT IN AN ORBITAL MAY BE A BONDING ELECTRON PAIR OR A LONE ELECTRON PAIR WHICH DOES NOT FORM A BOND. </li></ul><ul><li>(5) ALL BONDS DO NOT REQUIRE HYBRIDIZATION IN ORDER TO FORM. </li></ul>
  26. 26. HYBRIDIZATION AND PERIODIC TRENDS <ul><li>TRENDS IN BONDING BETWEEN ATOMS OCCUR IN SIMILAR FASHION AMONG MEMBERS OF THE SAME CHEMICAL FAMILY (COLUMNS ON THE PERIODIC TABLE). </li></ul><ul><li>THE BONDING CHARACTERISTICS OF EACH FAMILY ON THE PERIODIC TABLE ARE DEMONSTRATED IN THE FOLLOWING FRAMES. </li></ul><ul><li>ALTHOUGH ELEMENTS IN A FAMILY GENERALLY DO ACT SIMILARLY, NOT ALL THE ELEMENTS IN A PARTICULAR FAMILY ACT IN EXACTLY THE SAME WAY. </li></ul>
  27. 27. UNHYBRIDIZED LITHIUM (BEFORE REACTING) 3P 2S 1S Li LITHIUM LITHIUM WITH NO HYBRIDIZATION (CAPABLE OF FORMING ONE BOND) NO ELECTRON PROMOTION OR HYBRIDIZATION OCCURS H BONDING ORBITAL WHEN BONDS FORM WITH HYDROGEN (H 1s 1 ) COMPOUND LiH RESULTS
  28. 28. UNHYBRIDIZED BERYLLIUM (BEFORE REACTING) 3P 2S 1S Be BERYLLIUM SP HYBRID ORBITALS BERYLLIUM IN HYBRIDIZED STATE (CAPABLE OF FORMING TWO BONDS) ELECTRON PROMOTION AND HYBRIDIZATION OCCURS H H WHEN BONDS FORM WITH HYDROGEN (H 1s 1 ) BONDING ORBITALS COMPOUND BeH 2 RESULTS
  29. 29. UNHYBRIDIZED BORON (BEFORE REACTING) 3P 2S 1S B BORON SP 2 HYBRID ORBITALS BORON IN HYBRIDIZED STATE (CAPABLE OF FORMING THREE BONDS) ELECTRON PROMOTION AND HYBRIDIZATION OCCURS H H H WHEN BONDS FORM WITH HYDROGEN (H 1s 1 ) BONDING ORBITALS COMPOUND BH 3 RESULTS
  30. 30. UNHYBRIDIZED CARBON (BEFORE REACTING) 3P 2S 1S C CARBON SP 3 HYBRID ORBITALS CARBON IN HYBRIDIZED STATE (CAPABLE OF FORMING FOUR BONDS) ELECTRON PROMOTION AND HYBRIDIZATION OCCURS H H H H WHEN BONDS FORM WITH HYDROGEN (H 1s 1 ) COMPOUND CH 4 RESULTS BONDING ORBITALS
  31. 31. UNHYBRIDIZED NITROGEN (BEFORE REACTING) 3P 2S 1S N NITROGEN SP 3 HYBRID ORBITALS NITROGEN IN HYBRIDIZED STATE (CAPABLE OF FORMING THREE BONDS WITH ONE LONE ELECTRON PAIR) ELECTRON PROMOTION AND HYBRIDIZATION OCCURS H H H WHEN BONDS FORM WITH HYDROGEN (H 1s 1 ) COMPOUND NH 3 RESULTS BONDING ORBITALS LONE e - PAIR
  32. 32. UNHYBRIDIZED OXYGEN (BEFORE REACTING) 3P 2S 1S O OXYGEN SP 3 HYBRID ORBITALS OXYGEN IN HYBRIDIZED STATE (CAPABLE OF FORMING TWO BONDS WITH TWO LONE ELECTRON PAIRS) ELECTRON PROMOTION AND HYBRIDIZATION OCCURS H H WHEN BONDS FORM WITH HYDROGEN (H 1s 1 ) COMPOUND H 2 O RESULTS BONDING ORBITALS TWO LONE e - PAIRS
  33. 33. UNHYBRIDIZED CARBON (BEFORE REACTING) 3P 2S 1S F FLOURINE SP 3 HYBRID ORBITALS FLOURINE IN HYBRIDIZED STATE (CAPABLE OF FORMING ONE BOND WITH THREE LONE ELECTRON PAIRS) ELECTRON PROMOTION AND HYBRIDIZATION OCCURS H WHEN BONDS FORM WITH HYDROGEN (H 1s 1 ) COMPOUND HF RESULTS THREE LONE e - PAIRS BONDING ORBITALS
  34. 34. N . . . . . H . . H H . H + AMMONIA NH 3 HYDROGEN ION WITH NO ELECTRONS COORDINATE COVALENT BOND FORMATION H + AMMONIUM ION IS FORMED NH 4 + LONE e- PAIR
  35. 35. THE END
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