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Kinetics II

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Total cards: 16•Content version: v4•Public deck•Updated: 8/1/2026

Card preview (16)

#1
Front (Question)

What is the rate equation?

Back (Answer)

• k[A]^m[B]^n

#2
Front (Question)

how will a conc-rate graph look for a 0 order reaction?

Back (Answer)

• Flat line (m of 0)

#3
Front (Question)

How will a con-rate graph look for a 1st order reaction?

Back (Answer)

• straight line going through the origin (positive m)

#4
Front (Question)

How will a con-rate graph look for a 2nd order reaction?

Back (Answer)

• exponential graph with a positive m

#5
Front (Question)

What does it tell us if half lives of a conc-time graph are constant?

Back (Answer)

its 1st order

#6
Front (Question)

What does it tell us if half lives of a conc-time graph are rapidly increasing (or vary very weirdly?)

Back (Answer)

its 2nd order

#7
Front (Question)

What does it tell us if half lives of a conc-time graph are a straight line with a negative m?

Back (Answer)

it is 0 order

#8
Front (Question)

what are the units of an overall reaction of 2nd order?

Back (Answer)

mol^-1dm^3s^-1

#9
Front (Question)

what are the units of an overall reaction of 1st order?

Back (Answer)

s^-1

#10
Front (Question)

what are the units of an overall reaction of 3rd order?

Back (Answer)

• mol^-2dm^6s^-1

#11
Front (Question)

give some key points of Sn1 reactions?

Back (Answer)

• only have 1 molecule or ion in the rate determining step (rate equation) • tertiary or secondary haloalkanes react through this mechanism

#12
Front (Question)

Describe Sn1 reactions

Back (Answer)

• curly arrow from middle of C-X bond to X- • forms a carbocation with a X- • OH- ion attacks carbocation (which will be a positive)

#13
Front (Question)

Describe Sn2 reactions

Back (Answer)

• forms an intermediate from nucleophillic substitution (kind of like a halogen and OH- competing for the spot) • HAPPENS IN ONE STEP

#14
Front (Question)

Give some key points of Sn2 reactions

Back (Answer)

• only 1 rate determining step • have 2 molecules or ions in the rate determining step. ( rate equation)

#15
Front (Question)

Why do tertiary haloalkanes proceed via Sn1 reactions?

Back (Answer)

• Because there is less space around their alkyl groups (they’re larger) for nucleophiles to attack,

#16
Front (Question)

Back (Answer)