html5-img
1 / 11

Organics – Naming the Molecules

Organics – Naming the Molecules. Types Chain lengths Add–ons Specific naming . Naming - Introduction. In organic chemistry the names of each molecules has three main parts: The type of chemical e.g. Alkane The length of its longest carbon chain The add–ons to the main chain of carbons

zoie
Download Presentation

Organics – Naming the Molecules

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Organics – Naming the Molecules Types Chain lengths Add–ons Specific naming

  2. Naming - Introduction • In organic chemistry the names of each molecules has three main parts: • The type of chemical e.g. Alkane • The length of its longest carbon chain • The add–ons to the main chain of carbons • When we put them together into the name we use the order: Add–on : Length of chain : Type of organic • To make life interesting, we give codes to help us so that we don’t have to write: One chlorine is attached to the second carbon in a chain five carbons long in an alkane

  3. Naming - Types • As we have seen already there are a few different types of organic chemicals. Each one is given a specific code name that gets tacked on as a suffix (end of a word)

  4. Naming – Chain Length • The organic molecules can come in a number of lengths e.g. 1 carbon, 2 carbons… • The number of carbons in the main chain of the molecule forms a prefix (beginning of a word) for the name

  5. Naming – Add-ons I • The main chain can have stuff added to it. These might be extra carbon branches or halogens. It is important for us to be able to know exactly what and where they are. • This forms the very first part of the name (before the prefix). Here is how we do it: • Count the number of carbons in from the closest side (along the main chain). This forms the number that goes at the front of the name • Next write the code for the add-on e.g. 2 methyl pentane

  6. Naming – Add-ons II • Some times they add more than on add-on. This means that the name needs to show us how many there are and where we can find them. • To do this we need to: • Add all the numbers showing where each add-on is found • Sometimes the add-on code needs a prefix telling us how many there are e.g. 2,3 dimethyl butane

  7. Practice

  8. Specific Naming Rules– Alkenes and Alkynes • Some types have extra part to their name specifically telling us where certain features can be found: • Alkenes – we need to know where the double bond is. In this case we count in from the closest side – if the double bond is on the first bond of a pentene we would call it pent-1-ene • Alkynes – the same rule applies e.g. oct-3-yne

  9. Specific Naming Rules – Alkanols (Alcohols) • Naming and alcohol is very similar to naming alkenes and alkynes. This is because the location of the –OH group on the chain is very important • In this case we number the carbon (from the closest end) and locate which carbon the –OH is on. • For example, ‘propan-1-ol’ means that the –OH is on the first (number 1) carbon. ‘Propan-2-ol’ has the –OH on the second carbon • Why is there no such chemical as ‘propan-3-ol’ ?

  10. Specific Naming Rules - Esters • Esters are made when we react an alcohol with a carboxylic acid. • Unfortunately they are difficult to name because they have a break in their carbon chain. We therefore have to add two parts to their name: • The part from the alcohol comes first. Its name comes from how many carbons it has e.g. methyl, ethyl, propyl… etc • The part from the carboxylic acid comes last. It ends in ‘-oate’ e.g. methanoate, ethanoate, propanoate… etc. You can always tell which part came from an acid, because acids have more oxygen atoms Acid half = butanoate Alcohol half = ethyl Ethylbutanoate

  11. Practice II

More Related