(See attached file for full problem description)
a. The structure of 1,3-butadiene is usually written as H2C==CH--CH==CH2. The average bond lengths given are: C--C of 154pm and C==C of 133pm. Explain the fact that the observed value of the distance between the two central carbon atoms in 1,3-butadiene is 146pm.
b. Which of the attached three possible resonance structures would make the greatest contribution to the resonance hybrid? Explain your answer.
c. Cinnamaldehyde (structure attached) gives the spice cinnamon its characteristic odor. How many signma bonds and how many pi bonds are in this molecule?© BrainMass Inc. brainmass.com September 19, 2018, 4:32 pm ad1c9bdddf - https://brainmass.com/chemistry/organic-chemistry-bonding/resonance-structures-bond-lengths-types-molecules-93322
Please the attached file for your answers.
1. The bond length between the central Carbon atoms in butadiene is less than 154 and more than 133 pm which means it is a bond with a bond order between 1 and 2. We can say this as the bond is between a double bond and a single bond. This is actually the case in butadiene. The electron density is delocalized between all the 4 ...
Three questions on bond structures, resonance structures, and the types of bonds within the given molecule structures.