Difference between revisions of "GChemPaint/C3/Resonance-Structures/English"
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| − | Title of the tutorial: ''' | + | Title of the tutorial: '''Resonance Structures''' |
Author: '''Madhuri Ganapathi''' | Author: '''Madhuri Ganapathi''' | ||
| − | Key words:''' Molecular contextual menu,Chemical calculator, Composition, Isotropic pattern, video tutorial''' | + | Key words: ''' Molecular contextual menu,Chemical calculator, Composition, Isotropic pattern, video tutorial''' |
| Line 17: | Line 17: | ||
||Hello everyone. | ||Hello everyone. | ||
| − | Welcome to this tutorial on ''' | + | Welcome to this tutorial on '''Resonance Structures''' in '''GChemPaint'''. |
|- | |- | ||
||'''Slide Number 2''' | ||'''Slide Number 2''' | ||
'''Learning Objectives''' | '''Learning Objectives''' | ||
| − | ||In this tutorial, we will learn | + | ||In this tutorial, we will learn to, |
| − | + | ||
| − | + | ||
| − | + | ||
| − | + | ||
| − | + | ||
| − | + | ||
| − | + | ||
| + | * Use different types of arrows to represent chemical reactions | ||
| + | *Add charge and electron pairs on an atom | ||
| + | |- | ||
| + | ||Slide Number 3 | ||
| + | System Requirement | ||
| + | ||For this tutorial I am using | ||
| + | Ubuntu Linux OS version 12.04. | ||
| + | GChemPaint version 0.12.10. | ||
| + | |- | ||
| + | ||Slide Number 4 | ||
| + | Pre-requisites | ||
| + | ||To follow this tutorial you should be familiar with GchemPaint. | ||
| + | If not,Switch to GChemPaint window. | ||
| + | ||I will switch to GChemPaint window. | ||
| + | Here you can see EthylChloride and Methylbromide structures. | ||
| + | for relevant tutorials, please visit our website. | ||
| + | |- | ||
| + | || | ||
| + | ||I will show how to obtain a Carbo-cation. | ||
| + | |- | ||
| + | ||Point to Chlorine atom. | ||
| + | ||Let's add a pair of electrons on the Chlorine atom of EthylChloride. | ||
| + | |- | ||
| + | ||Click on Add an electron pair to an atom tool>>Click on Chlorine atom. | ||
| + | ||Click on Add an electron pair tool. | ||
| + | Click on Chlorine atom and observe what happens. | ||
| + | |- | ||
| + | || | ||
| + | ||Next, I will show an electron pair shift in the Carbon-Chlorine bond. | ||
| + | |- | ||
| + | ||Click on Add a curved arrow to represent an electron pair move. | ||
| + | Point to the window. | ||
| + | ||Click on Add a curved arrow to represent an electron pair move. | ||
| + | Property window opens. | ||
| + | |- | ||
| + | ||Click on''' End arrow at center of new bond''' check box. | ||
| + | ||Click on '''End arrow at center of new bond''' check box. | ||
| + | |- | ||
| + | ||Click on Carbon-Chlorine bond. | ||
| + | ||Click on Carbon-Chlorine bond. | ||
| + | It moves the electron pair to the correct position. | ||
| + | |- | ||
| + | ||Point to the shift. | ||
| + | ||Place the cursor on the curved arrow and observe the electron shift. | ||
| + | |- | ||
| + | ||Point to the structure. | ||
| + | ||I will the copy of the structure. | ||
| + | |- | ||
| + | ||Click on Add on arrow and click between the structures. | ||
| + | ||Now, click on Add on arrow and click between the structures. | ||
| + | |- | ||
| + | || | ||
| + | ||Formation of a Carbo-cation is initialized by a base like Sodium Hydroxide(NaOH). | ||
| + | |- | ||
| + | ||Click on Add or modify a group of atoms tool and click above the arrow. | ||
| + | ||Click on Add or modify a group of atoms tool and click above the arrow. | ||
| + | |- | ||
| + | ||Type NaOH in the green box. | ||
| + | ||Type NaOH in the green box. | ||
| + | |- | ||
| + | ||Click on Selection tool>>Click on the text Base to select>>Right-click click on the arrow. | ||
| + | ||Click on Selection tool and select NaOH. | ||
| + | Then, right-click on the arrow. | ||
| + | |- | ||
| + | ||Point to the submenu. | ||
| + | Select Arrow >>click on Attach selection to arrow. | ||
| + | ||In the submenu, select Arrow. | ||
| + | Click on Attach selection to arrow. | ||
| + | |- | ||
| + | ||Point to the dialogue box. | ||
| + | || | ||
| + | A dialogue box with heading Arrow associated appears. | ||
| + | |- | ||
| + | ||Point to drop down. | ||
| + | ||In Role drop-down, select “Reactant” and click on Close. <PAUSE> | ||
| + | |- | ||
| + | || | ||
| + | ||Now, let's convert second EthylChloride to Ethyl Carbo-cation and Chloride ions. | ||
| + | |- | ||
| + | ||Click on Eraser tool and click on Carbon-chlorine bond. | ||
| + | Point to products. | ||
| + | ||Click on Eraser tool and click on Carbon-chlorine bond. | ||
| + | Ethane(CH3-CH3) and HCl are formed. | ||
| + | |- | ||
| + | ||Point to the central carbon. | ||
| + | ||When electrons shift from Carbon to Chlorine, Carbon gains a positive charge. | ||
| + | |- | ||
| + | ||Click on Increment the charge of an atom tool>>Click at the position from where Carbon-chlorine bond to deleted. | ||
| + | ||Click on Increment the charge tool. | ||
| + | Click at the position from where Carbon-chlorine bond was deleted. | ||
| + | Ethyl Carbo-cation(CH3-CH2+) is formed. | ||
| + | |- | ||
| + | ||click on Decrement the charge of an atom tool>>click on HCl. | ||
| + | ||To form Chloride ion, click on Decrement the charge tool. | ||
| + | Click on HCl. | ||
| + | Chloride(Cl-) ion is formed. | ||
| + | <PAUSE> | ||
| + | |- | ||
| + | ||Point to Current element drop down arrow button. | ||
| + | ||Now let's move to single electron shift. | ||
| + | |- | ||
| + | ||Point to Methylbromide. | ||
| + | ||Let's use the Methylbromide structure to obtain free radicals. | ||
| + | |- | ||
| + | ||Click on Add a curved arrow to represent a single electron move tool. | ||
| + | ||Click on Add a curved arrow to represent a single electron move tool. | ||
| + | |- | ||
| + | ||Click twice on Bromo-methane bond. | ||
| + | ||Click on Methylbromide bond to obtain a curved arrow. | ||
| + | Shift the Pencil tool a little on the bond, click again to get second curved arrow. | ||
| + | |- | ||
| + | ||Point to the Bromo-methane and curved arrows. | ||
| + | ||One curved arrow moves to bromo(Br) and other moves towards methyl(CH3). | ||
| + | Both Bromo(Br) and methyl(CH3 ) will get one electron each from the bonded pair. | ||
| + | |- | ||
| + | ||Point to the arrow. | ||
| + | ||To show the products, let's add an arrow. | ||
| + | Click on Add an arrow click on Display area. | ||
| + | |- | ||
| + | ||Point to the free radicals. | ||
| + | ||Formation of free radicals involves heat in the reaction. | ||
| + | |- | ||
| + | ||Click on Add or modify a text tool. | ||
| + | Click on the Display area above the arrow. Type “Heat” in the green box. | ||
| + | ||Click on Add or modify a text tool. | ||
| + | Click on Display area above the arrow. | ||
| + | Type “Heat” in the green box. | ||
| + | |- | ||
| + | ||Click on Selection tool>>select “Heat”. | ||
| + | ||Click on Selection tool and select “Heat” | ||
| + | |- | ||
| + | ||Right-click on the arrow. | ||
| + | Point to the submenu>> Select Arrow >>click on Attach selection to arrow. | ||
| + | ||Right-click on the arrow. | ||
| + | In the Submenu select Arrow. | ||
| + | Click on Attach selection to arrow. | ||
| + | |- | ||
| + | ||Point to the dialogue box. | ||
| + | || | ||
| + | A dialogue box with heading Arrow associated appears. | ||
| + | |- | ||
| + | ||Point to drop down. | ||
| + | ||Notice that Role drop down list has more options. | ||
| + | |- | ||
| + | ||Point to Role drop down. | ||
| + | Select “Temperature”>>Click on Close. | ||
| + | ||In the Role drop-down, select “Temperature” and click on Close. | ||
| + | |- | ||
| + | ||Point to the structure. | ||
| + | ||I will copy the structure. | ||
| + | |- | ||
| + | || | ||
| + | ||Now let's create the free radicals. | ||
| + | |- | ||
| + | ||Click on Eraser tool and click on Carbon-bromine bond. | ||
| + | Point to CH4 and HBr. | ||
| + | ||Click on Eraser tool and click on Carbon-bromine bond. | ||
| + | Methane(CH4) and Hydrogen-bromide(HBr) are formed. | ||
| + | |- | ||
| + | ||Click on Add an upaired electron tool. | ||
| + | Click on CH4 and HBr. | ||
| + | ||Click on Add an upaired electron tool. | ||
| + | Click on Methane(CH4) and Hydrogen-bromide(HBr) | ||
| + | Methyl(CH3) and Bromium(Br^-) free radicals are formed. | ||
| + | |- | ||
| + | || | ||
| + | ||Let's create a reaction pathway. | ||
| + | |- | ||
| + | ||Click on Selection tool. | ||
| + | Drag the cursor over the reaction to select it. | ||
| + | ||Click on Selection tool. | ||
| + | To create a reaction pathway, first select the complete reaction. | ||
| + | |- | ||
| + | ||Right-click on the selection. | ||
| + | Point to the Submenu. | ||
| + | ||Now, right-click on the selection. | ||
| + | A submenu opens. | ||
| + | |- | ||
| + | ||Click on Create a new reaction. | ||
| + | Point to the previous reaction | ||
| + | ||Click on Create a new reaction. | ||
| + | Reaction path is created. | ||
| + | Drag to see the reaction pathway. | ||
| + | Likewise, I will create the reaction pathway for the previous reaction. | ||
| + | |- | ||
| + | ||Right-click on the selection again. | ||
| + | Click on Destroy the reaction. | ||
| + | ||We can also remove the reaction pathway, if we want to. | ||
| + | To do so, right-click on the reaction again and click on Destroy the reaction. | ||
| + | |- | ||
| + | ||Point to the reactants and products. | ||
| + | Drag any object. | ||
| + | ||This action will remove the reaction pathway. | ||
| + | Drag any of the objects, and you will see that they can be moved individually. | ||
| + | |- | ||
| + | || | ||
| + | ||Now we move on to Resonance or mesomery using double headed arrow. | ||
| + | |- | ||
| + | ||Switch to GChempaint. | ||
| + | Point to the structureCH3-NH2). | ||
| + | ||I have opened a new GChemPaint window with structures of Nitromethane. | ||
| + | |- | ||
| + | ||Point to the structures | ||
| + | ||I had added curved arrows and charges to show electron shifts within the structures. | ||
| + | |- | ||
| + | || | ||
| + | || | ||
| + | Now let's add a double headed arrow. | ||
| + | |- | ||
| + | ||Click on Add a double headed arrow. | ||
| + | Click on Display area beside Nitromethane. | ||
| + | ||Click on Add a double headed arrow. | ||
| + | Click on Display area in between Nitromethanes. | ||
| + | |- | ||
| + | ||Point to the structures | ||
| + | ||The two structures are canonical forms of Nitromethane. | ||
| + | |- | ||
| + | ||Press CTRL+A to select the structures. | ||
| + | Right-click on the selection. | ||
| + | Point to the Submenu. | ||
| + | ||Press CTRL+A to select the structures. | ||
| + | Right-click on the selection. | ||
| + | A submenu opens. | ||
| + | |- | ||
| + | ||Click on Create a new mesomery relationship | ||
| + | ||Click on Create a new mesomery relationship. | ||
| + | Drag to see the relationship. | ||
| + | |- | ||
| + | ||Slide Number | ||
| + | Resonance structures of Benzene | ||
| + | ||Here is slide for resonance structures of Benzene. | ||
| + | |- | ||
| + | || | ||
| + | ||Now, let's learn to create a retro-synthetic pathway. | ||
| + | |- | ||
| + | ||Point to the window. | ||
| + | ||I have opened a new GChemPaint window with the required structures. | ||
| + | |- | ||
| + | ||Point to the final product intermediates and starting material. | ||
| + | ||Retrosynthetic pathway | ||
| + | starts with the product | ||
| + | and goes to the reactant | ||
| + | along with all the intermediates. | ||
| + | |- | ||
| + | ||Point to the structures | ||
| + | ||In this pathway, the final product is Orthonitrophenol and the starting material is Benzene. | ||
| + | |- | ||
| + | || | ||
| + | || | ||
| + | Let's add a retro-synthetic arrow, to show the retro-synthetic pathway. | ||
| + | |- | ||
| + | ||Click on Add arrow for a retrosynthetic step >> Click in between all the compounds. | ||
| + | ||Click on Add arrow for a retrosynthetic step. | ||
| + | Click in between all the compounds. | ||
| + | |- | ||
| + | ||Press CTRL+A select all structures. | ||
| + | Right click on the selection. | ||
| + | ||Press CTRL+A select all structures. | ||
| + | Right click on the selection. | ||
| + | |- | ||
| + | ||Point to Submenu. | ||
| + | Click on Create a new retrosynthesis pathway. | ||
| + | ||A sub-menu opens. | ||
| + | Click on Create a new retrosynthesis pathway. | ||
| + | Drag to see the created pathway. | ||
| + | |- | ||
| + | || | ||
| + | ||Let's summarize what we have learnt. | ||
| + | |- | ||
| + | ||Slide Number 9 | ||
| + | Summary | ||
| + | ||In this tutorial we have learnt to | ||
| + | Show electron shifts using curved arrows | ||
| + | Attach reaction conditions to reaction arrows. | ||
| + | Create and destroy reaction pathway using a reaction arrow | ||
| + | Create a new mesomery relationship using double headed arrow | ||
| + | Create a retro-synthetic pathway using the retro-synthetic arrow. | ||
| + | |- | ||
| + | ||Slide Number 10 | ||
| + | Assignment | ||
| + | ||As an assignment | ||
| + | Using arrow properties | ||
| + | 1. Create a reaction pathway for the reaction between Bromo-Ethane (C2H5Br) and Sodium(Na) with Dry ether as a solvent to obtain Butane(C4H10) and Sodium bromide(NaBr). | ||
| + | 2. Add stoichiometric coefficients to the reactants and products. | ||
| + | 3. Draw resonance structures of Naphtalene, Anthracene and Carbondioxide | ||
| + | |- | ||
| + | ||Point to the reaction pathway. | ||
| + | Point to the resonance structures | ||
| + | || | ||
| + | This is the required reaction pathway. | ||
| + | These are the resonance structures of Napthalein, Anthracene and Carbondioxide. | ||
| + | |- | ||
||'''Slide Number 10''' | ||'''Slide Number 10''' | ||
Revision as of 11:27, 28 April 2014
Title of the tutorial: Resonance Structures
Author: Madhuri Ganapathi
Key words: Molecular contextual menu,Chemical calculator, Composition, Isotropic pattern, video tutorial
| Visual Cue | Narration
| |
|---|---|---|
| Slide Number 1
Title Slide |
Hello everyone.
Welcome to this tutorial on Resonance Structures in GChemPaint. | |
| Slide Number 2
Learning Objectives |
In this tutorial, we will learn to,
| |
| Slide Number 3
System Requirement |
For this tutorial I am using
Ubuntu Linux OS version 12.04. GChemPaint version 0.12.10. | |
| Slide Number 4
Pre-requisites |
To follow this tutorial you should be familiar with GchemPaint.
If not,Switch to GChemPaint window. |
I will switch to GChemPaint window.
Here you can see EthylChloride and Methylbromide structures. for relevant tutorials, please visit our website. |
| I will show how to obtain a Carbo-cation. | ||
| Point to Chlorine atom. | Let's add a pair of electrons on the Chlorine atom of EthylChloride. | |
| Click on Add an electron pair to an atom tool>>Click on Chlorine atom. | Click on Add an electron pair tool.
Click on Chlorine atom and observe what happens. | |
| Next, I will show an electron pair shift in the Carbon-Chlorine bond. | ||
| Click on Add a curved arrow to represent an electron pair move.
Point to the window. |
Click on Add a curved arrow to represent an electron pair move.
Property window opens. | |
| Click on End arrow at center of new bond check box. | Click on End arrow at center of new bond check box. | |
| Click on Carbon-Chlorine bond. | Click on Carbon-Chlorine bond.
It moves the electron pair to the correct position. | |
| Point to the shift. | Place the cursor on the curved arrow and observe the electron shift. | |
| Point to the structure. | I will the copy of the structure. | |
| Click on Add on arrow and click between the structures. | Now, click on Add on arrow and click between the structures. | |
| Formation of a Carbo-cation is initialized by a base like Sodium Hydroxide(NaOH). | ||
| Click on Add or modify a group of atoms tool and click above the arrow. | Click on Add or modify a group of atoms tool and click above the arrow. | |
| Type NaOH in the green box. | Type NaOH in the green box. | |
| Click on Selection tool>>Click on the text Base to select>>Right-click click on the arrow. | Click on Selection tool and select NaOH.
Then, right-click on the arrow. | |
| Point to the submenu.
Select Arrow >>click on Attach selection to arrow. |
In the submenu, select Arrow.
Click on Attach selection to arrow. | |
| Point to the dialogue box. |
A dialogue box with heading Arrow associated appears. | |
| Point to drop down. | In Role drop-down, select “Reactant” and click on Close. <PAUSE> | |
| Now, let's convert second EthylChloride to Ethyl Carbo-cation and Chloride ions. | ||
| Click on Eraser tool and click on Carbon-chlorine bond.
Point to products. |
Click on Eraser tool and click on Carbon-chlorine bond.
Ethane(CH3-CH3) and HCl are formed. | |
| Point to the central carbon. | When electrons shift from Carbon to Chlorine, Carbon gains a positive charge. | |
| Click on Increment the charge of an atom tool>>Click at the position from where Carbon-chlorine bond to deleted. | Click on Increment the charge tool.
Click at the position from where Carbon-chlorine bond was deleted. Ethyl Carbo-cation(CH3-CH2+) is formed. | |
| click on Decrement the charge of an atom tool>>click on HCl. | To form Chloride ion, click on Decrement the charge tool.
Click on HCl. Chloride(Cl-) ion is formed. <PAUSE> | |
| Point to Current element drop down arrow button. | Now let's move to single electron shift. | |
| Point to Methylbromide. | Let's use the Methylbromide structure to obtain free radicals. | |
| Click on Add a curved arrow to represent a single electron move tool. | Click on Add a curved arrow to represent a single electron move tool. | |
| Click twice on Bromo-methane bond. | Click on Methylbromide bond to obtain a curved arrow.
Shift the Pencil tool a little on the bond, click again to get second curved arrow. | |
| Point to the Bromo-methane and curved arrows. | One curved arrow moves to bromo(Br) and other moves towards methyl(CH3).
Both Bromo(Br) and methyl(CH3 ) will get one electron each from the bonded pair. | |
| Point to the arrow. | To show the products, let's add an arrow.
Click on Add an arrow click on Display area. | |
| Point to the free radicals. | Formation of free radicals involves heat in the reaction. | |
| Click on Add or modify a text tool.
Click on the Display area above the arrow. Type “Heat” in the green box. |
Click on Add or modify a text tool.
Click on Display area above the arrow. Type “Heat” in the green box. | |
| Click on Selection tool>>select “Heat”. | Click on Selection tool and select “Heat” | |
| Right-click on the arrow.
Point to the submenu>> Select Arrow >>click on Attach selection to arrow. |
Right-click on the arrow.
In the Submenu select Arrow. Click on Attach selection to arrow. | |
| Point to the dialogue box. |
A dialogue box with heading Arrow associated appears. | |
| Point to drop down. | Notice that Role drop down list has more options. | |
| Point to Role drop down.
Select “Temperature”>>Click on Close. |
In the Role drop-down, select “Temperature” and click on Close. | |
| Point to the structure. | I will copy the structure. | |
| Now let's create the free radicals. | ||
| Click on Eraser tool and click on Carbon-bromine bond.
Point to CH4 and HBr. |
Click on Eraser tool and click on Carbon-bromine bond.
Methane(CH4) and Hydrogen-bromide(HBr) are formed. | |
| Click on Add an upaired electron tool.
Click on CH4 and HBr. |
Click on Add an upaired electron tool.
Click on Methane(CH4) and Hydrogen-bromide(HBr) Methyl(CH3) and Bromium(Br^-) free radicals are formed. | |
| Let's create a reaction pathway. | ||
| Click on Selection tool.
Drag the cursor over the reaction to select it. |
Click on Selection tool.
To create a reaction pathway, first select the complete reaction. | |
| Right-click on the selection.
Point to the Submenu. |
Now, right-click on the selection.
A submenu opens. | |
| Click on Create a new reaction.
Point to the previous reaction |
Click on Create a new reaction.
Reaction path is created. Drag to see the reaction pathway. Likewise, I will create the reaction pathway for the previous reaction. | |
| Right-click on the selection again.
|
We can also remove the reaction pathway, if we want to.
To do so, right-click on the reaction again and click on Destroy the reaction. | |
| Point to the reactants and products.
Drag any object. |
This action will remove the reaction pathway.
Drag any of the objects, and you will see that they can be moved individually. | |
| Now we move on to Resonance or mesomery using double headed arrow. | ||
| Switch to GChempaint.
Point to the structureCH3-NH2). |
I have opened a new GChemPaint window with structures of Nitromethane. | |
| Point to the structures | I had added curved arrows and charges to show electron shifts within the structures. | |
|
Now let's add a double headed arrow. | ||
| Click on Add a double headed arrow.
Click on Display area beside Nitromethane. |
Click on Add a double headed arrow.
Click on Display area in between Nitromethanes. | |
| Point to the structures | The two structures are canonical forms of Nitromethane. | |
| Press CTRL+A to select the structures.
Right-click on the selection. Point to the Submenu. |
Press CTRL+A to select the structures.
Right-click on the selection. A submenu opens. | |
| Click on Create a new mesomery relationship | Click on Create a new mesomery relationship.
Drag to see the relationship. | |
| Slide Number
Resonance structures of Benzene |
Here is slide for resonance structures of Benzene. | |
| Now, let's learn to create a retro-synthetic pathway. | ||
| Point to the window. | I have opened a new GChemPaint window with the required structures. | |
| Point to the final product intermediates and starting material. | Retrosynthetic pathway
starts with the product and goes to the reactant along with all the intermediates. | |
| Point to the structures | In this pathway, the final product is Orthonitrophenol and the starting material is Benzene. | |
|
Let's add a retro-synthetic arrow, to show the retro-synthetic pathway. | ||
| Click on Add arrow for a retrosynthetic step >> Click in between all the compounds. | Click on Add arrow for a retrosynthetic step.
Click in between all the compounds. | |
| Press CTRL+A select all structures.
Right click on the selection. |
Press CTRL+A select all structures.
Right click on the selection. | |
| Point to Submenu.
Click on Create a new retrosynthesis pathway. |
A sub-menu opens.
Click on Create a new retrosynthesis pathway. Drag to see the created pathway. | |
| Let's summarize what we have learnt. | ||
| Slide Number 9
Summary |
In this tutorial we have learnt to
Show electron shifts using curved arrows Attach reaction conditions to reaction arrows. Create and destroy reaction pathway using a reaction arrow Create a new mesomery relationship using double headed arrow Create a retro-synthetic pathway using the retro-synthetic arrow. | |
| Slide Number 10
Assignment |
As an assignment
Using arrow properties 1. Create a reaction pathway for the reaction between Bromo-Ethane (C2H5Br) and Sodium(Na) with Dry ether as a solvent to obtain Butane(C4H10) and Sodium bromide(NaBr). 2. Add stoichiometric coefficients to the reactants and products. 3. Draw resonance structures of Naphtalene, Anthracene and Carbondioxide | |
| Point to the reaction pathway.
Point to the resonance structures |
This is the required reaction pathway. These are the resonance structures of Napthalein, Anthracene and Carbondioxide. | |
| Slide Number 10
Acknowledgement |
Watch the video available at this URL.
http://spoken-tutorial.org/What_is_a_Spoken_ Tutorial It summarizes the Spoken Tutorial project If you do not have good bandwidth, you can download and watch it | |
| Slide Number 11 | The Spoken Tutorial Project Team:
Conducts workshops using spoken tutorials Gives certificates to those who pass an on-line test For more details, please write to contact@spoken-tutorial.org | |
| Slide number 12 | Spoken Tutorial Project is a part of the Talk to a Teacher project
It is supported by the National Mission on Education through ICT, MHRD, Government of India More information on this Mission is available at this link | |
| This is Madhuri Ganapathi from IIT Bombay signing off. Thank you for joining. |