by Karson Fiallos https://padlet.com/karsonfiallos12/2k5xs7hwhdhreo1m Hecho con un poco de aventura en-us 2022-05-19 00:44:15 UTC 2026-01-05 05:39:43 UTC hello@padlet.com Alkene karsonfiallos12 https://padlet.com/karsonfiallos12/2k5xs7hwhdhreo1m/wish/2190359329
 homologous series of hydrocarbons that contain a carbon-carbon double bond. The number of hydrogen atoms in an alkene is double the number of carbon atoms, so they have the general formula CnH2n.


]]> 2022-05-19 00:48:02 UTC https://padlet.com/karsonfiallos12/2k5xs7hwhdhreo1m/wish/2190359329 Alkene Structure karsonfiallos12 https://padlet.com/karsonfiallos12/2k5xs7hwhdhreo1m/wish/2190382881 As noted before, alkenes are hydrocarbons with carbon-to-carbon double bonds (H2C=CH2) ]]> 2022-05-19 01:06:44 UTC https://padlet.com/karsonfiallos12/2k5xs7hwhdhreo1m/wish/2190382881 Uses karsonfiallos12 https://padlet.com/karsonfiallos12/2k5xs7hwhdhreo1m/wish/2190464729 Used in:
1. Synthesis of alcohols 
2. Plastics 
3. Lacquers 
4. Detergents 
5. Fuels as starting materials. ]]> 2022-05-19 02:01:43 UTC https://padlet.com/karsonfiallos12/2k5xs7hwhdhreo1m/wish/2190464729 Physical Properties karsonfiallos12 https://padlet.com/karsonfiallos12/2k5xs7hwhdhreo1m/wish/2190491780 1. Physical State
2. Solubility
3. Boiling Point
4. Melting Point
5. Polarity





]]> 2022-05-19 02:19:06 UTC https://padlet.com/karsonfiallos12/2k5xs7hwhdhreo1m/wish/2190491780 Common Reactions karsonfiallos12 https://padlet.com/karsonfiallos12/2k5xs7hwhdhreo1m/wish/2190498691 -Halogenation 
-Hydrogenation 
-Oxidation 
-Hydration]]> 2022-05-19 02:23:27 UTC https://padlet.com/karsonfiallos12/2k5xs7hwhdhreo1m/wish/2190498691 Interesting Facts karsonfiallos12 https://padlet.com/karsonfiallos12/2k5xs7hwhdhreo1m/wish/2190550784
  • All the alkenes with 4 or more carbon atoms in them show structural
  • The carbon-carbon double bond doesn't allow any rotation about it, (cis-trans isomerism).
  • Shared electrons in the double bond are called pi electrons and they create a pi bond.
  • The electrons in the pi bond are free to move around anywhere in this shaded region and can move freely from one half to the other.
  • The rather exposed electrons in the pi bond are particularly open to attack by things which carry some degree of positive charge. These are called



    • ]]>     2022-05-19 03:00:05 UTC https://padlet.com/karsonfiallos12/2k5xs7hwhdhreo1m/wish/2190550784     Structures karsonfiallos12 https://padlet.com/karsonfiallos12/2k5xs7hwhdhreo1m/wish/2190556699 2022-05-19 03:03:59 UTC https://padlet.com/karsonfiallos12/2k5xs7hwhdhreo1m/wish/2190556699 References karsonfiallos12 https://padlet.com/karsonfiallos12/2k5xs7hwhdhreo1m/wish/2190565248 https://www.bbc.co.uk/bitesize/guides/z3mpk7h/revision/4#:~:text=Alkenes%20are%20a%20homologous%20series,C%20n%20H%202%20n%20.

    https://chem.libretexts.org/Bookshelves/Introductory_Chemistry/The_Basics_of_GOB_Chemistry_(Ball_et_al.)/13%3A_Unsaturated_and_Aromatic_Hydrocarbons/13.01%3A_Alkenes-_Structures_and_Names

    https://byjus.com/chemistry/alkene/#:~:text=What%20are%20alkenes%20used%20for,and%201%2C3-butadiene.

    https://byjus.com/chemistry/physical-properties-of-alkenes/

    https://www.studysmarter.us/explanations/chemistry/organic-chemistry/reactions-of-alkenes/#:~:text=Four%20common%20reactions%20involving%20alkenes,hydrogenation%2C%20oxidation%2C%20and%20hydration.

    https://alevelchemistry.co.uk/notes/alkenes/



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