**Physical Description:** This substance is a colorless but fragrant liquid that is oily in appearance.**Chemical Information:**- **Observed Melting Point:** -78.5 °C- **Observed Boiling Point:** 138-142 °C- **Calculated Molecular Weight (MW):** 130 g/mol- **Density:** 0.876 g/cm³- **Solubility in Water:** Minimally soluble- **Other Property:** Flash Point: 77 °F**Spectroscopic Information:** Infrared (IR) bands indicate this compound contains C-H functionalities, with a strong stretch near 1700 cm⁻¹ and several strong bands between 1500 and 1000 cm⁻¹.**IR Spectrum Description:** The graph shows a spectrum with peaks consistent with C-H functional groups, a notable stretch at approximately 1700 cm⁻¹, and additional strong peaks in the range of 1500 to 1000 cm⁻¹. **NMR Information:**- The ¹³C NMR spectrum for this compound indicates six unique carbon atoms and no cyclic structure.- The proton NMR data reveal five sets of unique protons.**C-13 NMR Data:**- 171.08 ppm (Intensity: 222)- 63.13 ppm (Intensity: 887)- 37.48 ppm (Intensity: 645)- 25.18 ppm (Intensity: 635)- 22.51 ppm (Intensity: 100) - 9.96 ppm (Intensity: 473)**H-1 NMR Data:**- Signal A: 4.095 ppm- Signal B: 2.037 ppm- Signal C: 1.693 ppm- Signal D: 1.521 ppm- Signal E: 0.926 ppmThis comprehensive analysis provides insight into the compound's structural and functional properties, essential for understanding its chemical behavior and applications.

A question is based on physical and chemical information and IR and NMR spectroscopy.Based on the…

Physical description: This substance is a colorless but fragrant liquid that is oily in appearance. Chemical information: Observed Melting point: -78.5 °C Observed Boiling point: 138-142 °C Calculated MW: 130 g/mol Density: 0.876 g/cm³ Solubility in water: Minimally soluble, Other: Flash Point: 77 °F Spectroscopic information: IR bands indicate this compound contains C-H functionalities and the appearance of a strong stretch near 1700 cm³¹ as well as several strong bands between 1500 and 1000 cm-¹. 4600 171.08 222 63.13 887 37.48 645 25.18 635 3000 22.51 1000 20.96 473 The 13C NMR spectrum for this compound indicates 6 unique carbon atoms and no cyclic structure. The proton NMR data indicate 5 sets of unique protons. C-13 data: ppm Int. Assign. 1 423456 VENUMBER H-1 data: Assign. 1000 ABCDE Shift (ppm) 4.095 2.037 1.693 1.521 0.926

Physical description: This substance is a colorless but fragrant liquid that is oily in appearance. Chemical information: Observed Melting point: -78.5 °C Observed Boiling point: 138-142 °C Calculated MW: 130 g/mol Density: 0.876 g/cm³ Solubility in water: Minimally soluble, Other: Flash Point: 77 °F Spectroscopic information: IR bands indicate this compound contains C-H functionalities and the appearance of a strong stretch near 1700 cm³¹ as well as several strong bands between 1500 and 1000 cm-¹. 4600 171.08 222 63.13 887 37.48 645 25.18 635 3000 22.51 1000 20.96 473 The 13C NMR spectrum for this compound indicates 6 unique carbon atoms and no cyclic structure. The proton NMR data indicate 5 sets of unique protons. C-13 data: ppm Int. Assign. 1 423456 VENUMBER H-1 data: Assign. 1000 ABCDE Shift (ppm) 4.095 2.037 1.693 1.521 0.926

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Similar questions

1. Is this molecule is saturated? Explain your reasoning. нннн Н-с—С—С-с-н H HHH
Please don't provide handwriting solution
Data for Problem 2 ZOO 180 150 120 140 100 80 770 дом -8 60 40 20 10 9 a 5 015 100 80 Relative Intensity 8 ส 20 20 40 50 ppm septet 3 2 60 70 80 90 100 m/z
IR spectra is unique to a particular molecule. The spectra in the region of 1500-4000 cm 1 region, provides clear information about the functional groups present. This area is known as the O analytical region O fingerprint region O diagnostic region O absorption region
https://drive.google.com/file/d/14UPPDWhJXm0KKcLAOXDyBULvI_sISzDW/view?usp=sharing Which hazard statement is false in regards to dichloromethane? 1) May be corrosive to metals 2) Causes skin irritation 3) Causes serious eye irritation 4) Suspected of causing cancer
Pretty sure they are all wrong ?
4. Below are the structures of some medications. Circle and identify functional groups in the structures. H₂C H₂C core MDPV Mephedrone 'N H CH3 Cocaine CH3 CH3 Methylone CH3 Aom CH3 CH3 CH3 Amphetamine NH₂ но... HO HO LaH O ACO OH 10-deacetylbaccatin III
Chloroform CHCl3 is your compound saturated or unsaturated? Do any geometric isomers exist in point format what functional groups does your chemical contain in point format And add any other information that you learned about chloroform in point format
List the name and position for each substituent in this organic molecule on a separate row of the table below: CH3 Q-CH₂-CH3 CH3–CH–CH2–CH-CH=CH2–CH2–CH3 CH₂-CH₂-CH3 Your answer for the name column should be just one word. In the position column, write the number of the carbon where the substituent is attached to the parent chain (which has been highlighted for you). Note for advanced students: You may assume that the parent chain is numbered from left-to-right in this molecule. You can add more rows to the table if you need them. name Add Row position 0 X
What functional groups can be found on the molecule below. Choose all that apply:(Vanillin, vanilla extract) Alcohol Aromatic Carboxylic Acid Ether Aldehyde