Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
25 Cards in this Set
- Front
- Back
IR tells you...
|
types of bonds.
|
|
(IR) Carbonyls absorb at ...
|
~1750 cm⁻¹
|
|
(IR) X-axis ranges from...
|
400 to 4000 cm⁻¹
|
|
(IR) OH groups absorb at...
|
~3300 cm⁻¹ (broad)
|
|
(IR) Amines absorb at...
|
~3000 cm⁻¹ (sharp)
|
|
(IR) Is the N-H or C-H peak typically further left?
|
N-H
|
|
(NMR) Nuclei align w/ or against ...
|
external magnetic fields.
|
|
(NMR) Flipping nuclei alignment to against results in...
|
high energy state.
|
|
(NMR) Downfield =
|
more deshielded.
|
|
(NMR) De-shielded =
|
proximity to e⁻ w/drawing groups.
|
|
(NMR) H bonded to sp³ C puts peak bw...
|
0 and 5 ppm.
|
|
(NMR) H bonded to sp² C puts peak bw...
|
5 and 10 ppm.
|
|
(NMR) Nuclei w/magnetic moments have...
|
odd-numbered masses or odd atomic numbers.
|
|
C NMR ranges up to...
|
100 ppm.
|
|
(NMR) Spin-coupled C NMR has...
|
splitting.
|
|
(NMR) Spin-decoupled C NMR has...
|
no splitting.
|
|
UV-Vis examines...
|
conjugated systems.
|
|
Which type of spectroscopy destroys the sample?
|
Mass spectroscopy.
|
|
Which types of spectroscopy use light?
|
IR, NMR, UV
|
|
What does a mass spectroscopy detector detect?
|
mass/charge ratio
|
|
(MS) Base peak represents...
|
most abundant ion.
|
|
Parent peak (M+) represents...
|
molecular weight of original molecule.
|
|
(NMR) Splitting requires...
|
multiple peaks.
|
|
(NMR) When protons are all equivalent, you see...
|
no splitting.
|
|
(NMR) Aromatic ring peaks found bw...
|
6 and 8 ppm
|