The structure below is Technetium-99mTriamide-Mercaptide. what is the shape of the compound, and how do the oxo-ligands bind in the body for renal nuclear imaging?
The structure below is Technetium-99mTriamide-Mercaptide. what is the shape of the compound, and how do the...
Technetium Dosage. Radioactive isotopes are often used for medical imaging. Technetium-99m (Tc-99m) is a particularly popular isotope since it has a short half-life and is easy to make. Also, Tc-99m can be chemically bonded to a number of different compounds and cell types for imaging different parts of the body. Tc-99m has a half-life of 6.02 hours. It decays into Tc-99 by emitting a gamma ray of energy 140 keV. For this problem, assume that Tc-99m is present in the...
5. What is the shape around each carbon atom in the structure shown below? The shape around each carbon atom is tetrahedral. The shape around each carbon atom is bent. The shape around the left carbon atom is tetrahedral and bent around the right carbon atom. The shape around the left carbon atom is trigonal planar and linear around the right carbon atom A) B) C) D)
Draw the Skeletal Structure of the Unknown Compound, with NMR given below. Information: Each spectra below was obtained from a pure compound. Mass Spectrum parent peaks (M) are listed for all examples. IR peaks listed are strong (s) unless otherwise indicated for signals above 1500 cm "H NMR Spectra, the integral is given in number of hydrogens #H) or as a relative ratio. Important coupling constants U-values) are listed next to the peaks for some examples. For some spectra, an...
Draw the structure of the compound that is consistent with the H NMR data below. Do not draw ar hydrogens in your solution. It must be drawn as a true skeletal structure 3 molecular formula chemical shift (ppm) relative integration multiplicity C5H100 1.50 doublet 1.61 doublet 2.85 broad singlet 3.91 multiplet 5.21-5.40 multiplet
Draw the Skeletal Structure of the unknown compound. Formal skeletal structures do not include hydrogens on any carbons (including the aldehyde C). Mass Spectrometry (not shown): [M] = 122 (100%), [M+2] = 124 (100%) m/z Infrared Spectroscopy (not shown): 2988, 2973 cm 'H Nuclear Magnetic Resonance. ET 3 PPM 2H 2 GH " Nuclear Magnetic Resonance. Mass Spectrometry (not shown): [M] = 147 (100%), (M+2] = 149 (100%) m/z Infrared Spectroscopy (not shown): 2969, 2935, 2249 cm 'H Nuclear Magnetic...
Draw the Skeletal Structure of the Unknown Compound, with NMR given below Information: Each spectra belaw was obtained from a pure compound. Mass Spectrum parent peaks (M) are listed for all examples. IR peaks listed are strong is) unless otherwise indicated for signals above 1500 cm 'H NMR Spectra, the integral is given in number of hydrogens (WH) or as a relative ratio. Important coupling constants (-values) are listed next to the peaks for some examples. For some spectra, an...
1. What did you notice about the shapes with and without the lone pairs? how do the lone lairs affect the final shape? Guidelines for Drawing Lewis Structures. STEP 1: Determine the total number of valence electrons for the molecule. STEP 2: Determine the skeletal structure arrangement of atoms) of the compound. For simple compounds the singular atom will be in the center with the others arranged around it. STEP 3: Attach each bonded atom to the central atom with...
13C and 1H NMR spectra of a compound, C10H14, are displayed below. What is the structure of the compound? Explain. Note: This same question was asked here: http://www.chegg.com/homework-help/questions-and-answers/13c-1h-nmr-spectra-compound-c10h14-displayed--structure-compound-explain-please-explain-q3820429 As pointed out, the structure is C10H14 and the answered offered had 11 carbons.
Draw the Skeletal Structure of the Unknown Compound. Note - Formal skeletal structures do not include hydrogens on any carbons (including the aldehyde C) Information: Each spectra below was obtained from a pure compound, Mass Spectrum parent peaks (M) are listed for all examples. IR peaks listed are strong (s) unless otherwise indicated for signals above 1500 cm 'H NMR Spectra, the integral is given in number of hydrogens (#H) or as a relative ratio. Important coupling constants (J-values) are...
Draw the Skeletal Structure of the Unknown Compound. Note - Formal skeletal structures do not include hydrogens on any carbons (including the aldehyde C). Information: Each spectra below was obtained from a pure compound. Mass Spectrum parent peaks (M) are listed for all examples. IR peaks listed are strong (s) unless otherwise indicated for signals above 1500 cm 'H NMR Spectra, the integral is given in number of hydrogens (#H) or as a relative ratio. Important coupling constants (J-values) are...