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      <title>Remake of PH1125- UNIT 1- DISCUSSION BOARD by </title>
      <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k</link>
      <description>Please enter here your questions/doubt etc about the content of PH1125 unit 1 content</description>
      <language>en-us</language>
      <pubDate>2020-11-09 10:27:20 UTC</pubDate>
      <lastBuildDate>2023-01-27 23:47:52 UTC</lastBuildDate>
      <webMaster>hello@padlet.com</webMaster>
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      <item>
         <title>What does sp3 mean?</title>
         <author>pertusatif</author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603959</link>
         <description><![CDATA[]]></description>
         <enclosure url="" />
         <pubDate>2020-11-09 10:27:20 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603959</guid>
      </item>
      <item>
         <title>Chemdraw</title>
         <author>pertusatif</author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603962</link>
         <description><![CDATA[<div>Hi. I have installed ChemDraw 16.0. For the activation, it asks for a serial number and I'm not sure where to find it. Thanks. <br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2020-11-09 10:27:20 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603962</guid>
      </item>
      <item>
         <title>Chemdraw Video</title>
         <author>pertusatif</author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603963</link>
         <description><![CDATA[<div>Hi, I'm trying to install Chemdraw but the video on learning central is down. I'm unable to view it to follow the steps required to properly install Chemdraw. How can I go about solving this issue?<br>Thanks.<br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2020-11-09 10:27:20 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603963</guid>
      </item>
      <item>
         <title>Questions for Tutorial</title>
         <author>pertusatif</author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603964</link>
         <description><![CDATA[<div>Are we meant to use the Chemdraw software to draw the molecules for the first few questions or can we draw them on paper and take a photo to send them in? </div>]]></description>
         <enclosure url="" />
         <pubDate>2020-11-09 10:27:20 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603964</guid>
      </item>
      <item>
         <title>Hello, sorry to bother you but in lesson one </title>
         <author>pertusatif</author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603966</link>
         <description><![CDATA[]]></description>
         <enclosure url="" />
         <pubDate>2020-11-09 10:27:20 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603966</guid>
      </item>
      <item>
         <title>Tutorial Questions</title>
         <author>pertusatif</author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603968</link>
         <description><![CDATA[<div>Hi there, can anyone help me with Q4, the one where we have to say if the structures are mostly planar or non-planar?</div>]]></description>
         <enclosure url="" />
         <pubDate>2020-11-09 10:27:20 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603968</guid>
      </item>
      <item>
         <title>i thought hydrogen bond can only ne with N,O,F i dont undesrtand how it can form with S for like shown in the Hydrogen Bond donor example</title>
         <author>pertusatif</author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603971</link>
         <description><![CDATA[]]></description>
         <enclosure url="" />
         <pubDate>2020-11-09 10:27:20 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603971</guid>
      </item>
      <item>
         <title>Part 1 slideshow</title>
         <author>pertusatif</author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603972</link>
         <description><![CDATA[<div>Hi can you please upload the slideshow presentation to part 1.</div>]]></description>
         <enclosure url="" />
         <pubDate>2020-11-09 10:27:20 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603972</guid>
      </item>
      <item>
         <title>Part 1 presentation</title>
         <author>pertusatif</author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603975</link>
         <description><![CDATA[<div>Would you be able to upload the presentation for part 1 please to make it easier to make notes. Thanks</div>]]></description>
         <enclosure url="" />
         <pubDate>2020-11-09 10:27:20 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603975</guid>
      </item>
      <item>
         <title></title>
         <author>pertusatif</author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603979</link>
         <description><![CDATA[<div>hi yes there are no powerpoint slides for lesson 1<br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2020-11-09 10:27:20 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603979</guid>
      </item>
      <item>
         <title></title>
         <author>pertusatif</author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603980</link>
         <description><![CDATA[<div>could someone explain the resonance and inductive effect?</div>]]></description>
         <enclosure url="" />
         <pubDate>2020-11-09 10:27:20 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603980</guid>
      </item>
      <item>
         <title>extra slides</title>
         <author>pertusatif</author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603982</link>
         <description><![CDATA[<div>should we make notes on the slides added on the first part of the lesson but were not covered in the video</div>]]></description>
         <enclosure url="" />
         <pubDate>2020-11-09 10:27:20 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603982</guid>
      </item>
      <item>
         <title>Which FG will make a molecule lipophilic?</title>
         <author>pertusatif</author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603983</link>
         <description><![CDATA[<div>I don't understand why you said these cannot hydrogen bond?</div>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/762070973/4e30c584bd34ef2549067d3a08d3c0eb/Screenshot_2020_10_25_205015.png" />
         <pubDate>2020-11-09 10:27:20 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603983</guid>
      </item>
      <item>
         <title>Slides </title>
         <author>pertusatif</author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603985</link>
         <description><![CDATA[<div>hi, <br>from slide 25 onwards you haven't explained anything, there is no voice on the video, was this intentional? thankyou <br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2020-11-09 10:27:20 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603985</guid>
      </item>
      <item>
         <title>Where is the answer for the Hybrid Orbital formative questions?</title>
         <author>pertusatif</author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603991</link>
         <description><![CDATA[]]></description>
         <enclosure url="" />
         <pubDate>2020-11-09 10:27:20 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603991</guid>
      </item>
      <item>
         <title>Lesson 3 organic reaction mechanisms </title>
         <author>pertusatif</author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603992</link>
         <description><![CDATA[<div>Only  parts 2 and 3 have been uploaded. Is there a part 1 to this ?</div>]]></description>
         <enclosure url="" />
         <pubDate>2020-11-09 10:27:20 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603992</guid>
      </item>
      <item>
         <title>on the third video for organic reaction mechanisms, on slide 8 you say that E1 is the single concerted step. however, on slide 12 you say that the concerted reaction is E2. i am just wondering which step is correct.</title>
         <author>pertusatif</author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603994</link>
         <description><![CDATA[<div>Thanks </div>]]></description>
         <enclosure url="" />
         <pubDate>2020-11-09 10:27:20 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603994</guid>
      </item>
      <item>
         <title>Lesson 3 Part 1 Slide 11</title>
         <author>pertusatif</author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603997</link>
         <description><![CDATA[<div>Hi, on this slide C4H9Br is reacting with NH2-CH3. But when they react one of the Hs from NH2 goes missing? The product is shown as C4H9-NHCH3 but the other H isn't shown with the Br off to the side. I was just wondering if I had missed it somewhere?</div>]]></description>
         <enclosure url="" />
         <pubDate>2020-11-09 10:27:20 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603997</guid>
      </item>
      <item>
         <title>major product </title>
         <author>pertusatif</author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603998</link>
         <description><![CDATA[<div>could you explain please why that is the major product in slide 9 ? thank you<br><br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2020-11-09 10:27:20 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603998</guid>
      </item>
      <item>
         <title>Tutorial 3rd November 12am.</title>
         <author>pertusatif</author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603999</link>
         <description><![CDATA[<div>Hello,<br><br> I am unable to find Dr Claire Simon's e-mail address. Could someone help me? Also there is no zoom link in the session description for the tutorial.<br><br>Kind regards,<br><br>Michal Mlynarz. </div>]]></description>
         <enclosure url="" />
         <pubDate>2020-11-09 10:27:20 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903603999</guid>
      </item>
      <item>
         <title>Hi, </title>
         <author>pertusatif</author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903604001</link>
         <description><![CDATA[<div>Could you clarify E1 and E2 (in terms of how many steps there are in each etc). <br><br>Thanks!</div>]]></description>
         <enclosure url="" />
         <pubDate>2020-11-09 10:27:20 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903604001</guid>
      </item>
      <item>
         <title>Tutorial Questions</title>
         <author>pertusatif</author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903604002</link>
         <description><![CDATA[<div>I’ve completed the questions for the tutorial, do we need to submit our answers or just any questions that we had regarding the work? </div>]]></description>
         <enclosure url="" />
         <pubDate>2020-11-09 10:27:20 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903604002</guid>
      </item>
      <item>
         <title>SN1 and SN2</title>
         <author>pertusatif</author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903604004</link>
         <description><![CDATA[<div>just wanted to confirm does Sn1 always have multiple steps and never single and does Sn2 always have single steps and never multiple.</div>]]></description>
         <enclosure url="" />
         <pubDate>2020-11-09 10:27:20 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903604004</guid>
      </item>
      <item>
         <title>Bases</title>
         <author>pertusatif</author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903604005</link>
         <description><![CDATA[<div>do the protons which leave the same compound form a bond with the OH- ion or halide ion, or do they form a bond with the base.</div>]]></description>
         <enclosure url="" />
         <pubDate>2020-11-09 10:27:20 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903604005</guid>
      </item>
      <item>
         <title>Slide 8 part 3</title>
         <author>pertusatif</author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903604006</link>
         <description><![CDATA[<div>Firstly, are the labels the wrong way around e.g. E1 involves 2 steps not 1? secondly, I don't understand what the two species are which are involved in E2 because from this slide there are bases and electrophiles involved in both E1 and E2 mechanisms.</div>]]></description>
         <enclosure url="" />
         <pubDate>2020-11-09 10:27:20 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/903604006</guid>
      </item>
      <item>
         <title>Workbook Answers</title>
         <author>tilym</author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/912402446</link>
         <description><![CDATA[<div>Hi. Where can I find the answers to the PH1125 workbook questions for Unit 1? Thank you.</div>]]></description>
         <enclosure url="" />
         <pubDate>2020-11-11 11:34:28 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/912402446</guid>
      </item>
      <item>
         <title>Enol or Enolate</title>
         <author></author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/913412429</link>
         <description><![CDATA[<div>I was wondering why in the final product the alpha carbon is described as being from the enolate, which I don't understand as I thought Enols have the alcohol group attached.</div>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/762070973/6bec9916b1aaa64ff456d3b5c980b766/enol.png" />
         <pubDate>2020-11-11 16:30:04 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/913412429</guid>
      </item>
      <item>
         <title>lesson 5 answers</title>
         <author></author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/916333065</link>
         <description><![CDATA[<div>when will we have access to the answers for the quetions at the end of lesson 5</div>]]></description>
         <enclosure url="" />
         <pubDate>2020-11-12 13:34:30 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/916333065</guid>
      </item>
      <item>
         <title>Hello </title>
         <author></author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/994073337</link>
         <description><![CDATA[]]></description>
         <enclosure url="" />
         <pubDate>2020-12-07 14:15:38 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/994073337</guid>
      </item>
      <item>
         <title>sorry this is for the sterochemistry part </title>
         <author></author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/1149587092</link>
         <description><![CDATA[<div>when "opening the double bond" in giving priority. does this only apply to C atoms or can you do this for O atoms.<br>thank you. </div>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/775553274/89418ef4ea35b2cac59687b80b8fc869/Screenshot__15_.png" />
         <pubDate>2021-02-01 16:26:53 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/1149587092</guid>
      </item>
      <item>
         <title>Question 6 diastereomers</title>
         <author></author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/1164867189</link>
         <description><![CDATA[<div>Hello, I am a bit confused as to why the diastereomers for question 6 does not include A and C as well as B and D. Any help would be greatly appreciated! Thank you! </div>]]></description>
         <enclosure url="" />
         <pubDate>2021-02-04 17:04:36 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/1164867189</guid>
      </item>
      <item>
         <title>R/S configuration</title>
         <author></author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/1165208696</link>
         <description><![CDATA[<div>can someone please explain how to determine R/S. i dont quite understand! thanks guys </div>]]></description>
         <enclosure url="" />
         <pubDate>2021-02-04 18:01:28 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/1165208696</guid>
      </item>
      <item>
         <title>why do we open the door in cis and trans, how do we know when to apply the &#39;open the door&#39; method?</title>
         <author></author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/1174213821</link>
         <description><![CDATA[]]></description>
         <enclosure url="" />
         <pubDate>2021-02-07 19:08:25 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/1174213821</guid>
      </item>
      <item>
         <title>in the stereochemistry bit, it is said NH2 wins over C3 as the atomic number is higher in the NH2 ? but carbon has a higher atomic number than nitrogen? </title>
         <author></author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/1174322717</link>
         <description><![CDATA[]]></description>
         <enclosure url="" />
         <pubDate>2021-02-07 20:04:18 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/1174322717</guid>
      </item>
      <item>
         <title>workshop</title>
         <author></author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/1176625427</link>
         <description><![CDATA[<div>Do we need to bring anything to the stereochemistry workshop like our laptops, notes etc</div>]]></description>
         <enclosure url="" />
         <pubDate>2021-02-08 12:56:30 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/1176625427</guid>
      </item>
      <item>
         <title>hydride reduction</title>
         <author></author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/1502873443</link>
         <description><![CDATA[<div>Please can someone explain this slide. I get the first part of the mechanism but when it can attack anoo</div>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/1182897261/a02a2aa3933211931fb2664ab454eb23/Carbonyl_Compounds_Part_1.pptx" />
         <pubDate>2021-05-07 15:46:21 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/1502873443</guid>
      </item>
      <item>
         <title>Grignard</title>
         <author></author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/1502967053</link>
         <description><![CDATA[<div>Is R-MgBr the only grignard reagent or are their other?<br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2021-05-07 16:05:37 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/1502967053</guid>
      </item>
      <item>
         <title>Diasteromers &amp; enatiomers</title>
         <author></author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/1509669894</link>
         <description><![CDATA[<div>please can someone explain the difference, I really don't get the answers to the question on these? I think I get why A&amp;D; B&amp;C are enantiomers but I don't get the link between the diasteromers &amp; how you get to those answers</div>]]></description>
         <enclosure url="" />
         <pubDate>2021-05-10 15:31:39 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/1509669894</guid>
      </item>
      <item>
         <title> Amine Lecture</title>
         <author></author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/1560793262</link>
         <description><![CDATA[<div>I'm unsure about then formation of the least substituted alkane as the Hofmann Product. I don't understand how you know where the double bond will form?</div>]]></description>
         <enclosure url="" />
         <pubDate>2021-05-26 09:20:45 UTC</pubDate>
         <guid>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/1560793262</guid>
      </item>
      <item>
         <title>Quaternary carbon atoms</title>
         <author></author>
         <link>https://padlet.com/pertusatif/9zvwjkcy8y8kr34k/wish/1562755075</link>
         <description><![CDATA[<div>In one of the questions from the workshop, I can't find the quaternary carbon atom in flucloxacillin and amantadine? </div>]]></description>
         <enclosure url="" />
         <pubDate>2021-05-26 19:33:57 UTC</pubDate>
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