Miscellaneous Flashcards
What must always be included when writing formulae of IONS responsible for MOLECULAR ION peaks or fragment peaks
- a positive charge
-if the molecule wasn’t charged it wouldn’t be detected in the mass spectrometer
Ideal gas equation and units of each component
pV = nRT
p = pressure in pascals (Pa)
V = volume (m^3)
n= number of moles
R = gas constant (8.31 J mol^-1 K^-1)
T = temperature (Kelvin)
What is the danger of metal oxides
They are corrosive
Use of bumping granules
Provides a surface for bubbles to form on
Factors affecting Rf values
- different adsorption to stationary phase (chromatography paper)
-different solubility in the mobile phase
(Solvent)
What is the rate equation for Sn1 reactions
Rate = k [ tertiary halogenoalkane]
- as the slowest (rate-determining step) is the heterolytic fission of the R-X bond forming the carbocation intermediate
What is the rate equation for Sn1 reactions
• Rate = k [ tertiary carbocation]
• As slowest (rate-determining) step in Sn1, is homolytic fission of R-X bond to form carbocation intermediate
What is the rate equation for Sn1 reactions
• Rate = k [ tertiary halogenoalkane]
• As the slowest (rate-determining) step in Sn1 is homolytic fission of R-X bond to form carbocation intermediate
How can you make an reaction E cell reaction that isn’t feasible at standard conditions feasible?
-change the conditions
-so that you decrease or increase the standard electrode potential of one of your species
-so E cell is no longer negative
What is the rate equation for Sn2 reactions
- Rate = k [ primary halogenoalkane][nucleophile]
-As the slowest (rate-determining) step in Sn2 is the attack of the nucleophile on the halogenoalkane
Why are transition metalaqua ion complexes acidic in solution
-the small positively charged central metal cation polarises an O-H bond
-making it easier for water ligands to release hydrogen ions into solution
-metal aqua ions release protons in solution
Weak acid-strong base titration pH @ equivalent point
- pH >7
- @ equivalence point A- from ,weak acid ,HA react with water, releasing OH- ions into solution, making the pH at the equivalence point slightly basic
Strong acid-weak base titration pH @ equivalence point
-pH <7
-@ equivalence point salt made is slightly acidic (has a weak acidic), which partially dissociates at the equivalence point
What is region formed during the titration of a strong acid and a weak base
-Buffer Region
-When [HA] = [A-] , acting as reservoirs, neutralising added base
Why is standard enthalpy of Neutralisation for a weak acid less eco thermos than that or a strong acid
- weak acids do not fully ionise
-therefore more energy has to be put in /used to fully ionisie the acid