How to apply or use the give data when it come to Heats of Hydrogenation of Some Alkenes?

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How to apply or use the give data when it come to Heats of Hydrogenation of Some Alkenes

### Table: Heats of Hydrogenation of Alkenes

The table below presents the heat of hydrogenation (ΔH°_hydrog_) for various alkenes, measured in both kilojoules per mole (kJ/mol) and kilocalories per mole (kcal/mol). This data is crucial for understanding the stability of different alkenes based on their substitution patterns.

| Substitution     | Alkene                  | ΔH°_hydrog_ (kJ/mol) | ΔH°_hydrog_ (kcal/mol) |
|------------------|-------------------------|----------------------|------------------------|
| **Ethylene**     | H₂C=CH₂                 | −136                 | −32.6                  |
| **Monosubstituted** | CH₃CH=CH₂              | −125                 | −29.9                  |
| **Disubstituted** | CH₃CH=CHCH₃ (cis)       | −119                 | −28.3                  |
|                  | CH₃CH=CHCH₃ (trans)     | −115                 | −27.4                  |
|                  | (CH₃)₂C=CH₂             | −118                 | −28.2                  |
| **Trisubstituted**| (CH₃)₂C=CHCH₃          | −112                 | −26.7                  |
| **Tetrasubstituted** | (CH₃)₂C=C(CH₃)₂       | −110                 | −26.4                  |

### Explanation

- **Substitution:**
  - **Ethylene**: The most basic form of alkene with no additional carbon substituents.
  - **Monosubstituted:** One hydrogen atom in ethylene is replaced by a methyl group.
  - **Disubstituted:** Two hydrogen atoms are replaced by methyl groups. The table distinguishes between "cis" and "trans" forms and includes another variation with different substitution patterns.
  - **Trisubstituted:** Three hydrogen atoms are replaced by methyl groups.
  - **Tetrasubstituted:** All four hydrogen atoms are replaced by methyl groups.

- **Heat of Hydrogenation (ΔH°_hydrog_):** The energy released when an alkene is hydrogenated to an alkane.
  - **Stability Trend**: The
Transcribed Image Text:### Table: Heats of Hydrogenation of Alkenes The table below presents the heat of hydrogenation (ΔH°_hydrog_) for various alkenes, measured in both kilojoules per mole (kJ/mol) and kilocalories per mole (kcal/mol). This data is crucial for understanding the stability of different alkenes based on their substitution patterns. | Substitution | Alkene | ΔH°_hydrog_ (kJ/mol) | ΔH°_hydrog_ (kcal/mol) | |------------------|-------------------------|----------------------|------------------------| | **Ethylene** | H₂C=CH₂ | −136 | −32.6 | | **Monosubstituted** | CH₃CH=CH₂ | −125 | −29.9 | | **Disubstituted** | CH₃CH=CHCH₃ (cis) | −119 | −28.3 | | | CH₃CH=CHCH₃ (trans) | −115 | −27.4 | | | (CH₃)₂C=CH₂ | −118 | −28.2 | | **Trisubstituted**| (CH₃)₂C=CHCH₃ | −112 | −26.7 | | **Tetrasubstituted** | (CH₃)₂C=C(CH₃)₂ | −110 | −26.4 | ### Explanation - **Substitution:** - **Ethylene**: The most basic form of alkene with no additional carbon substituents. - **Monosubstituted:** One hydrogen atom in ethylene is replaced by a methyl group. - **Disubstituted:** Two hydrogen atoms are replaced by methyl groups. The table distinguishes between "cis" and "trans" forms and includes another variation with different substitution patterns. - **Trisubstituted:** Three hydrogen atoms are replaced by methyl groups. - **Tetrasubstituted:** All four hydrogen atoms are replaced by methyl groups. - **Heat of Hydrogenation (ΔH°_hydrog_):** The energy released when an alkene is hydrogenated to an alkane. - **Stability Trend**: The
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