Below is the Google document that serves as an outline for the group’s work and a storyboard for the video
Blog requirements:
The blog is composed of the following tabs:
- Introduction. This page should be use to introduce the topic of the group
- Chemical concept. Each group has explain in detail the chemical concept chosen by the group within the topic given to the group.
- Applications. Each group should chose one specific application of the chemical concept chosen.
- References. all the resources for the blog and the pictures have to be referenced.
- Assignments. Each weekly group assignment has to be uploaded before before the deadline.
- About the group. This space if for the group to introduce themselves in any fashion they want.
- Meeting logs. this tab is important for every group meeting regarding the group assignments. The groups have to meet to prepare their assignments and their multimedia project. The meeting log should contain (location, duration, participants and absentees, topics discussed, actions to be taken and by who before the next meeting, and any other relevant information that the group decides to document).
Idea for flow of storyboard
- Nuclear Magnetic Resonance (NMR) Spectroscopy
- Introduce what is nuclear magnetic resonance
- Electrons in molecules possess certain energy levels. i.e. quantized
- Change in energy levels by absorbing or releasing radiation
- Explain the equation E=hv
- Nuclei possess ‘spin’, denoted by quantum number I, and a very weak magnetic field is associated with it
- (Insert table of various nuclei with various quantum number and energy levels)
- Explain how there are 2I+1 number of orientations which each have different energy levels when in a magnetic field. Energy gap is proportional to strength of magnetic field
- when atoms are exposed to EM radiation of the right energy (ie resonant frequency), they can be promoted to the next energy level, resulting in a change in magnetic moment
- Spectroscopy
- atoms bonded to different things will experience varying amount of shielding/deshielding
- thus they will be in different magnetic environments and will have different resonant frequencies
- this unique resonant frequency can be compared with that of a reference compound, eg TMS
- Chemical Shift definition -> output of NMR is intensity against chemical shift
- Coupling: if neighbouring atoms have non-zero spin, they will carry a weak magnetic field and so their spin state will also affect the magnetic environment. As 2I+1 spin states are possible, a neigbour with spin I will split the signal into a set of 2I+1
- Eg: 1 neighbour with spin I=½ resulting in doublet
- most of the time this only occurs when I=½ as spin states rapidly interconvert (relaxation) when I is larger, causing net effect to average to zero. Only rarely does coupling occur, such as in the case of deuterium (I=1)
- Eg: 1 neighbour with spin I=1 resulting in triplet
- If there are multiple neighbours, the effect of the spin states may either reinforce each other or cancel out
- Eg: 2 equivalent neighbours with spin I=½ resulting in triplet
- Eg: 3 equivalent neighbours with spin I=½ resulting in quartet
- signal splits into 2nI+1 when there are n equivalent neighbours with I=I
- Coupling constant depends on strength of interaction. when coupling with non-equivalent neighbours, spin effects may not cancel out
- Eg: 2 non-equivalent neighbours with spin I=½ resulting in doublet of doublets
- Two common types of NMR spectroscopy: Carbon and Proton
- Explain what is the main difference then go into specifics
- Carbon NMR
- 13C vs 12C property
- Resonance at 2 quantized energy levels
- C-C then C-O then C=C then C=O (the 4 general groups)
- proton broadband decoupling
- why no C-C coupling
- Include one example
- Proton NMR
- Explain property is similar to 13C
- Concept of neighbour hydrogen and how it causes doublets, triplets, etc
- How the type of atom that the hydrogen is bonded to affects the frequency of resonance (carbon, oxygen, nitrogen or otherwise)
- Effects of multiple neighbours and different types of neighbours
- Include one example
- Further explanation
- Brief explanation of other types of NMR
- Possible Applications of NMR spectroscopy
- Explain how the application is useful in daily life
- Medicine – for medical diagnosis
- Chemistry – determining the molecular structure of compounds
- Non-destructive testing – expensive biological samples
- Any more?
Proposed Storyboard
Brief Introduction
| Shown on Screen | Explanation/Script |
| Introduction Header with Chocolate Pineapples |
Welcome to NMR Spectrocopy, brought to you by CHOCOLATE PINEAPPLES |
| Drawing of a compound entering a box stating NMR and signals leaving | NMR Spectronomy is used in modern chemistry to identify structural formula. By the difference and range of signals produced from the NMR, we can deduce the structural form of a certain compound. |
| A magnifying glass firstly showing a chocolate pineapple then zooming to pseudo nucleus of atom | To understand how NMR machines work, we need to go QUANTUM (Or molecular) |
Part 1: Concept of NMR
| Shown on screen | Explanation |
| Drawing of 1H with electron in magnetic field
Draw a H with arrows |
Physical phenomenon that nuclei resonates |
| Electromagnetic spectrum
Spectrum and zoom or bracket out spectrum |
NMR resonance falls under radio waves
(60MHz to 1000M cbn56y7Hz) |
| Energy levels for electron
E=hv equation |
Quantized energy levels for electron to promote, resulting in change in magnetic moment |
| Table of different atoms with different quantum spin number Said table |
Different atoms have different number of energy levels, not all can resonate |
| 2I + 1 equation | How to derive number of levels
Explain that NMR usually conducted on atoms with I=1/2, eg C13 and H |
| Diagram showing shielded/deshielded atoms | Explain chemical shift |
| Drawing of tetramethylsilane | Separation depends on magnetic field applied.
Use TMS as reference |
| Definition of chemical shift (Vreference) | Explain definition. Different atoms resonate at different frequencies, so Vref depends on what kind of NMR you want to do (choose the correct one from the reference compound, TMS) |
| Diagram showing the 2 states thing that results in coupling when I=1/2 | Coupling
coupling constant determined by the bond and frequency of resonance |
| Diagram showing the 3 states when I=1 | |
| Tree diagram for multiple coupling | Explain how to draw tree diagram based on constant J |
| Splitting equation 2nI+1 | Explain how to derive ratios for quantum spin number 1 and above (tree diagram) |
Part 2: Carbon NMR
| Shown on screen | Explanation |
| 2 drawings C-O and C-C | Not all carbon resonate at same frequency. |
| Diagram of relative shifts of C-X constituents
(side-by-side with previous diagram) |
Electron shielding effect on magnetic field affecting shift (downfield upfield) |
| C=C and C=O bonds | Use the cone thing to explain |
| 4 main bands | C-C / C-X / C=C / C=O |
| Proton decoupled C13-NMR vs non-decoupled | Explain most of the time, there is proton broadband decoupling (so that C-H coupling not shown) for clarity and speed of NMR |
| C13 vs C12 with percentages on screen | Relative rarity of C13, so no carbon-carbon coupling |
| Example: Sample molecule | Go through how to interpret chemical shift diagram |
Part 3: Proton NMR
| Shown on screen | Explanation |
| Ppm shifts for proton vs C13 | Why ppm shifts for proton are different |
| Relative shifts when attached (C, N, O) | Explain how the similar concept to C13 [magnetic field shift] |
| Molecule with neighbour hydrogens | Neighbour hydrogen and the effects on the peaks |
| Doublets Triplets Quartets | How to obtain number of peaks and naming and respective number of neighbours |
| Example: Sample molecule | Go through how to interpret chemical shift diagram |
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