(3E,5E)-octa-1,3,5,7-tetraene 1) How many atomic p orbitals does (35,5E)-octa-1,3,5,7-tetra ene have? 2) The atomic p orbitals...
9. Answer the questions below for 1,3,5,7-decatetraene. a. How many p atomic orbitals are in the conjugated system (draw)? b. How many molecular orbitals describe the conjugated system (draw)? c. How many molecular orbitals are bonding molecular orbitals? d. How many molecular orbitals are anti-bonding molecular orbitals? e. Which molecular orbitals are filled with electrons? f. If this molecule were to absorb a photon of UV light an electron would move between which two molecular orbitals (be specific)?
a. b. Answer the questions below for 1,3,5,7-decatetraene. How many p atomic orbitals are in the conjugated system (draw)? How many molecular orbitals describe the conjugated system (draw)? How many molecular orbitals are bonding molecular orbitals? d. How many molecular orbitals are anti-bonding molecular orbitals? e. Which molecular orbitals are filled with electrons? f. If this molecule were to absorb a photon of UV light an electron would move between which two molecular orbitals (be specific)?
Answer the questions below for 1,3,5,7-decatetraene. c. How many p atomic orbitals are in the conjugated system (draw)? b. How many molecular orbitals describe the conjugated system (draw)? How many molecular orbitals are bonding molecular orbitals? d. How many molecular orbitals are anti-bonding molecular orbitals? Which molecular orbitals are filled with electrons? f. If this molecule were to absorb a photon of UV light an electron would move between which two molecular orbitals (be specific)? e.
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Questions 1. Why does the trans conformation of a diene, in reaction with a dienophile, not lead to a Diels-Alder reaction product? 2. Complete the following Diels-Alder reactions. Provide the major endo-product(s). Diene Dienophile Product(s) Domov - 0.0- 3. How many a electrons are there in a molecule of 1.3-butadiene? 106 4. What is the maximum number of electrons that can reside in a molecular orbital? (Hint: It is the same maximum number that can fit into an...
How many molecular orbitals
are required for conjugated pi system in Vitamin D3? Draw the
orbitals in order of highest to lowest from top to bottom including
nodes. Label the HOMO and LUMO.
How many molecular orbitals are required for conjugated pi system in Vitamin D3? Draw the orbitals in order of highest to lowest from top to bottom including nodes. Label the HOMO and LUMO 2. HO ??, ??
QUESTION 1 For the following reaction, identify the 1,2-addition product. A) B) Br Br- Br + HBr C) D) Br ОООО С D 1 points QUESTION 2 Identify the product of the following reaction. + H,CO,C -CO,CH -CO,CH -CO_CH -CO,CH A CO,CH D) c) A) B) COACH CO,CH COCH, CO.CH B ОООО С D QUESTION 3 For (3E,5E)-octa-1,3,5,7-tetraene, shown below, how many of the a-molecular orbitals are bonding orbitals? 3 ОООО 6 PUS QUESTION 4 ОН ОН Which one of...
(a) Draw all of the pi molecular orbitals for (3E)-1, 3, 5-hexatriene ordering them from lowest to highest in energy. (b) Indicate which are bonding and which are antibonding. (c) Indicate the number of electrons that would be found in each in the ground state for the molecule. (d) Label the HOMO and LUMO.
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9. Answer the questions below for 1,3,5,7-decatetraene. a. How many p atomic orbitals are in the conjugated system (draw)? b. How many molecular orbitals describe the conjugated system (draw)? C. How many molecular orbitals are bonding molecular orbitals? d. How many molecular orbitals are anti-bonding molecular orbitals? e. Which molecular orbitals are filled with electrons? f. If this molecule were to absorb a photon of UV light an electron would move between which two...
1. a) What are the atomic orbitals that make up: i) Benzene: homo, lumo, homo-2, lumo+2 ii) Butadiene: homo, lumo, homo-1,lumo+1 iii) Formaldehyde: homo and lumo. - to what number molecular orbitals do these belong? iii) b) For the ten molecular orbitals of N2, what are their characteristics? What are the characteristics features of each bonding and antibonding orbital? How do the Pi 2p and the Pi*2p molecular orbitals differ in relative spatial orientation?