1. Gas chromatography is commonly used to _____________?
a) To check the purify of a volatile liquid sample, such as those obtained from a fractional distillation
b) To check the identity of an unknown substance by comparing its GC with the GC of a known
c) To analyze the components of a mixture for the presence or absence of a substance
2. All of the answers are applicable How many type of nonequivalent protons are in the following molecule? CH3CH2OCH2CH3
a) 1
b) 2
c) 3
d) 4
3. Which of the following is a factor that affects the 13C chemical shifts?
a) The electronegativity of the group attached to carbon
b) The atomic weight of the group attached to carbon
c) The hybridization of the hydrogen atoms
d) The number of hydrogen atom on an adjacent carbon atom
4. While 1H is the most abundant isotope of hydrogen, only ________% of the atom in carbon atoms in a sample are 13c
a) 1.1
b) 33
c) 50
d) 75
5. Where would you expect the peak for the benzyl cation (C6H5CH2+) to appear in mass spec?
a) m/z 77
b) m/z 108
c) m/z 91
d) m/z 17
6. Predict the splitting pattern for each kind of hydrogen in the following molecule (make splitting assignment starting with the group labeled as A followed by group B and then group C) (CH3)2CHCOOCH3-
A B C
a) A doublet; B multiplet; C, singlet
b) A doublet; B quartet; C singlet
c) A singlet; b multiplet; C doublet
d) A doublet; B doublet; C singlet
7. The role of drying agent is to ____ after the extraction process is complete?
a) Increase the solubility of the solute in the organic solvent
b) Remove trace amounts of water from the organic solvent
c) Remove huge amounts of water from the organic solvent
d) Increase the polarity of the aqueous layer
8. The carbon of ____ will appear the most downfield in the 13C NMR spectrum?
a) The carbonyl group
b) An aromatic ring
c) An alkene
d) An alkane
1. Gas chromatography is commonly used to _____________? a) To check the purify of a volatile...
Someone said it's not clear. Not sure what you're looking for. 4. a. For the molecule below, if simple splitting (follows the N+1 rule) occurs, Ha should appear as a (circle one: singlet, doublet, triplet, quartet) and Hb should appear as a (circle one: singlet, doublet, triplet, quartet) На 0 нь Hc b. Because Hb is attached to a chiral carbon atom, the molecule has diastereotopic Hs and the splitting becomes more complex. The nmr signal for Ha shows up...
and draw the Structures Determine the Hydrogen Deficiency Index Challenges: C4H8O2 1.2 8: 3H triplet 3.0 8: 2H quartet 3.6 8: 3H singlet CoH14 1.3 8: 9H singlet 7.2 8:5H multiplet C&H;N 3.7 8:2H singlet 7.2 8:5H singlet C.H.CI,O2 1.4 8: 3H triplet 4.3 8: 2H quartet 5.9 8: 1H singlet CsH1002 1.2 8:6H doublet 2.0 8:3H singlet 5.0 8: 1H septet 'H NMR Practice Problems Best thing is to first determine the Hydrogen Deficiency Index so you know the...
What splitting pattern in the 1H nmr spectrum would you expect for the hydrogen atom(s) colored red in the compounds shown below? The choices are: s singlet d doublet t triplet q quartet m multiplet. Enter the appropriate letter below each of the formulas. A B C D E F
can u pls answer all the questions 32. What is the expected splitting pattern for the indicated hydrogen? d. quartet a. Singlet b. Doublet C. Triplet e. quintet 33. What apparent splitting pattern would NOT be found in the 'H NMR spectrum for the following molecule? a. singlet w ord. quintet e. multiplet b. triplet c. quartet 34. Which of the following molecules would have a quartet at 3.5 ppm? но он
6. a. Which of the two labeled H atoms in each molecule absorbs farther downfield in 'H nmr? 0 H20-C-H b. Which of the two labeled C atoms in each molecule absorbs farther downfield in SC nmr? 0 0 H:O-C-H 7. The molecule shown below (directly above the spectrum) has four diffeent Hs (labeled A-D). ts 'H spectrum has four different nmr signals (labeled #1-#4). many neighbors? Hydrogen D matches signal # -. If you are undecided, look a. Hydrogens...
1. What splitting pattern in the 1H nmr spectrum would you expect for the hydrogen atom(s) colored red in the compounds shown below? Your choices are: s singlet d doublet t triplet quartet m multiplet. Enter the appropriate letter below each of the formulas. CH30-CH2-N(CH3)2 CH(CH3)2 -NO2 D (CH3)3c-O-CH2-CH3 E (CH3CH20)2CHCH3F
In a 13C NMR without 1H decoupling applied, a CH2 group will appear as a __________. Select the best answer. Select one: a. depends what is on the neighbouring atoms. b. triplet c. doublet d. quartet e. singlet
1) Nuclear magnetic resonance (NMR) spectroscopy can be used to gather information about the structure of a compound. The chemical shift of peaks in a 1H NMR or a 13C NMR spectrum can be used to gather information about the types of neighboring functional groups. The spin-spin splitting pattern in a 1H NMR spectrum can be used to determine the number of hydrogen atoms on neighboring carbon atoms. The chemical shift (?) of an atom is influenced by the electrons...
Identify the splitting pattern of the numbered protons. Atoms other than hydrogen and carbon are labeled. Select one: a. 1: quartet 2: quartet O b. 1: singlet, 2: triplet O c. 1: doublet, 2: triplet d. 1: triplet, 2: triplet
The H-NMR spectrum of an unknown compound (formula CaHgO2) is shown below. Draw the structure of the unknown compound. Question 5 4 1 6 5 8 10 11 Ppm The 13C-NMR spectrum of an unknown compound (formula CgH180) is shown below. Its 1H-NMR spectrum only shows one singlet at 1.2 ppm. Draw the structure of this unknown compound. uestion 2 220 200 160 140 120 PPM 100 80 240 180 60 40 20 Create OscerSketch Answer 2 What would be...