6. For the following polyunsaturated triglyceride: a) Label the indicated alkenes as cis or trans b) How many T bonds are the molecule? c) For the indicated bond, specify what orbitals are overlapping to form the bond. How many p bonds are in this molecule? (what orbitals are overlapping to form this bond?)

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**Analysis of Polyunsaturated Triglyceride**

**Instructions:**
1. Label the indicated alkenes as cis or trans.
2. Determine how many π bonds are in the molecule.
3. For the specified bond, identify which orbitals are overlapping to form the bond.

**Diagram Explanation:**
- The molecule diagram represents a polyunsaturated triglyceride with three highlighted sections requiring labeling of alkenes as either cis or trans.
- The structural formula includes a glycerol backbone connected to three fatty acid chains.
- Highlighted boxes point to carbon-carbon double bonds within the chains for cis/trans identification.
- A specific question asks for the total number of π bonds in the entire molecule.
- Another box prompts for identification of the orbitals overlapping in a specific bond, indicated by an arrow.

**Key Concepts:**
- *Cis/Trans Isomerism:* Alkenes can exhibit different spatial arrangements, known as isomers, which significantly impact the molecule's properties. "Cis" means the substituents are on the same side, while "trans" indicates they are on opposite sides.
- *π Bonds:* These are formed from the overlap of p orbitals, contributing to the double bond's strength and rigidity.
- *Orbital Overlap:* In the specified bond, determine which atomic orbitals are involved, typically involving p, sp, or sp2 hybridizations.
Transcribed Image Text:**Analysis of Polyunsaturated Triglyceride** **Instructions:** 1. Label the indicated alkenes as cis or trans. 2. Determine how many π bonds are in the molecule. 3. For the specified bond, identify which orbitals are overlapping to form the bond. **Diagram Explanation:** - The molecule diagram represents a polyunsaturated triglyceride with three highlighted sections requiring labeling of alkenes as either cis or trans. - The structural formula includes a glycerol backbone connected to three fatty acid chains. - Highlighted boxes point to carbon-carbon double bonds within the chains for cis/trans identification. - A specific question asks for the total number of π bonds in the entire molecule. - Another box prompts for identification of the orbitals overlapping in a specific bond, indicated by an arrow. **Key Concepts:** - *Cis/Trans Isomerism:* Alkenes can exhibit different spatial arrangements, known as isomers, which significantly impact the molecule's properties. "Cis" means the substituents are on the same side, while "trans" indicates they are on opposite sides. - *π Bonds:* These are formed from the overlap of p orbitals, contributing to the double bond's strength and rigidity. - *Orbital Overlap:* In the specified bond, determine which atomic orbitals are involved, typically involving p, sp, or sp2 hybridizations.
Expert Solution
Step 1

The type of alkenes (cis/trans), the number of π bonds are to be determined in the given trigyceride. What orbitals are overlapping in the indicated bond are to be specified.

The given triglyceride is,

Chemistry homework question answer, step 1, image 1

The alkenes are the compounds which have carbon - carbon double bond and indicated as C=C. The each C=C bond is made up of one sigma (σ) bond and one pi (π) bond. The each C=O bond also have one sigma (σ) bond and one pi (π) bond.

The type of orbitals overlapped in the particular bond can be determined from the hybridization of bonded atoms.

The alkenes or C=C bonds are of two types cis and trans. In cis form, the same priority groups are on same side of the plane of C=C bond and in trans form, the same priority groups are on opposite sides.

The CIP rules are nothing but Cahn–Ingold–Prelog priority rules are used to assign cis/trans descriptor to each double bond so that the configuration of the entire molecule can be specified.

The CIP priority rules:

  • The higher the atomic number, the higher the priority.
  • If two atoms have substituents of the same priority, higher priority is assigned to the atom with more of these substituents.
  • A larger group (i.e., more atoms) may not necessarily have a higher priority over another (smaller) group.
  • Atoms participating in double/triple bonds are considered to be bonded to an equivalent number of similar “phantom” atoms by single bonds.
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