1. Calculate the percentage s and p characters in sp, sp^2 and sp^3 hybrid orbitals. 2. Draw the molecular orbital diagram of propene, CH3-CH=CH2. 3. Draw an orbital diagram of an allene, H2C=C=CH2. What hybridization must the central carbon atom have in order to form two double bonds? 4. Describe the shape of sp^3 hybrid orbitals. 5. Dicuss, with illustrations, the two main steps in the hybridization of a carbon atom. 6.a. Arrange the following organic molecules in order of increasing acidity, starting with the least acidic. CH3CH3, HC(=_)CH and CH2=CH2 b. How many hybrid orbitals are formed when one 2s atomic orbital mixes with two 2p atomic orbitals? What shape do they form? c. Describe in detail, the shape of p atomic orbitals. d. Giving an example, explain what is meant by the excited-state electronic configuration of an atom of an element. e. Using clear illustrations, discuss the main differences between E1 and E2 mechanisms in organic reactions.

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1. Calculate the percentage s and p characters in sp, sp^2 and sp^3 hybrid orbitals. 2. Draw the molecular orbital diagram of propene, CH3-CH=CH2. 3. Draw an orbital diagram of an allene, H2C=C=CH2. What hybridization must the central carbon atom have in order to form two double bonds? 4. Describe the shape of sp^3 hybrid orbitals. 5. Dicuss, with illustrations, the two main steps in the hybridization of a carbon atom. 6.a. Arrange the following organic molecules in order of increasing acidity, starting with the least acidic. CH3CH3, HC(=_)CH and CH2=CH2 b. How many hybrid orbitals are formed when one 2s atomic orbital mixes with two 2p atomic orbitals? What shape do they form? c. Describe in detail, the shape of p atomic orbitals. d. Giving an example, explain what is meant by the excited-state electronic configuration of an atom of an element. e. Using clear illustrations, discuss the main differences between E1 and E2 mechanisms in organic reactions.
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