Determine the formula of the hydrocarbon compound where m/z=134. The mass spectrum indicates an M+2 peak in a 3:1 ratio. The IR spectrum also indicates a strong peak at 1760 cm1

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### Hydrocarbon Compound Analysis

**Problem Statement:**
Determine the formula of the hydrocarbon compound where m/z = 134. The mass spectrum indicates an M+2 peak in a 3:1 ratio. The IR spectrum also indicates a strong peak at 1760 cm⁻¹.

**Analysis:**
1. **Mass Spectrum Analysis:**
   - The mass spectrum of the compound shows a molecular ion peak (M) at m/z = 134.
   - The presence of an M+2 peak with a 3:1 ratio suggests the presence of chlorine (Cl) in the compound. Chlorine naturally occurs as two isotopes: ^35Cl and ^37Cl, with a relative abundance ratio of approximately 3:1.

2. **IR Spectrum Analysis:**
   - The IR spectrum shows a strong absorption peak at 1760 cm⁻¹. This is indicative of a carbonyl group (C=O), typically found in ketones, aldehydes, or esters.

**Conclusion:**
To find the formula, considering the presence of chlorine and a carbonyl group, and the molecular ion peak:
- Assuming the simplest structure, a mono-halogenated compound (one chlorine atom) with a carbonyl group, and calculating the rest of the molecular mass:

  The atomic mass of chlorine (^35Cl) is approximately 35.
  The mass of the remaining part of the molecule (134 - 35 = 99) should be composed of carbon (C), hydrogen (H), and oxygen (O) atoms.

For precise formula determination, the exact structure needs more details, but one plausible candidate is a compound like trichloroacetone (C3H3Cl3O).

**Answer:**
(Note: Depending on the educational focus, further study or details might be required to confirm and elaborate on the exact structure and formula.)

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Transcribed Image Text:### Hydrocarbon Compound Analysis **Problem Statement:** Determine the formula of the hydrocarbon compound where m/z = 134. The mass spectrum indicates an M+2 peak in a 3:1 ratio. The IR spectrum also indicates a strong peak at 1760 cm⁻¹. **Analysis:** 1. **Mass Spectrum Analysis:** - The mass spectrum of the compound shows a molecular ion peak (M) at m/z = 134. - The presence of an M+2 peak with a 3:1 ratio suggests the presence of chlorine (Cl) in the compound. Chlorine naturally occurs as two isotopes: ^35Cl and ^37Cl, with a relative abundance ratio of approximately 3:1. 2. **IR Spectrum Analysis:** - The IR spectrum shows a strong absorption peak at 1760 cm⁻¹. This is indicative of a carbonyl group (C=O), typically found in ketones, aldehydes, or esters. **Conclusion:** To find the formula, considering the presence of chlorine and a carbonyl group, and the molecular ion peak: - Assuming the simplest structure, a mono-halogenated compound (one chlorine atom) with a carbonyl group, and calculating the rest of the molecular mass: The atomic mass of chlorine (^35Cl) is approximately 35. The mass of the remaining part of the molecule (134 - 35 = 99) should be composed of carbon (C), hydrogen (H), and oxygen (O) atoms. For precise formula determination, the exact structure needs more details, but one plausible candidate is a compound like trichloroacetone (C3H3Cl3O). **Answer:** (Note: Depending on the educational focus, further study or details might be required to confirm and elaborate on the exact structure and formula.) [Answer Input Field]
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