answer all 3 questions pls In which region of the 13C NMR spectrum do you expect...
Which of the reagents listed below would efficiently accomplish the transformation of CH,CH,CH=CHCH,CH,CHO into CHỊCH,CH,CH,CH,CH,CH,OH? 4 Select one or more: Va. KMnO b. NaBH, c. Br in CCIA d. H. Ni Ve. Two of these choices
pls help. 13-15 pls
-C-C-H H is unusually acidic because the ion produced when it is lost is stabilized bg resonance, with one of the structures having a (A) I, + on C (B) 1. - ono (C) II, + on C (D) II, - on 0 CH2CH3 CHCH; СН,ОН HCOCH, HCOCH OH OCH This reaction needs catalyst. (A) an acid (B) a base (C) no (D) either an acid or a base au, ca eu (4) chach;& n ®...
27) The 'H NMR spectrum for p-ethylaniline is shown below. Which signal correlates to the indicated hydrogen atoms? 3H, triplet a) signal at ~2.6 ppm H₂N. b) signal at ~3.4 ppm 2H, 2H, doublet 2H, CH CH3 doublet quartet c) signal at ~6.6 ppm 2H d) signal at ~7.0 ppm 28) Select the major product of the following se howing series of reactions. 1) SOCl2 OH y So C, C1,CH. pyridine 2) CH3CH2CH2OH, pyridine OH OH oh odlom "D" transformation.
Could anybody help me answer the selected questions?
8.8 Identify the compounds of the given molecular formulas that show a. One 'H NMR signal: CHO CH C.H.Br, b. Two 'H NMR signals: CH.CL CHO CHO, CHOCI 8.9 8.10 How many 'H NMR signals will each of the compounds below show? a. (CH, CHỊCH, d. CH.COCH,CH.COCH, b. CH,COCOOCH, e. CH.COCH.CH.COOCH, c. CH,COCH,COCH, L. CHCOCH CH(CI)COCH, Suggest structures consistent with the following 'H NMR data: а. Сно CHCI triplet (1.0 ppm, 3H)...
which of the following would you expect to have a longer lambda
max? explain?
pls answer all the questions
Which of the following would you expect to have the longer Ama? Explain. 18. How can UV-visible spectroscopy be used to monitor a chemical reaction? 19. Which of the following would show a C-O stretch at the lowest frequency in its IR spectrum? 20. O NH2 ОН OCH3 I1 II IV V Which of the following would be likely to exhibit...
please help me answer the IR, H NMR and 13C NMR questions based
on the pictures below.
IR List the important peaks seen in the IR of the product and label with the associated stretches and bends (eg. C-H stretch, etc). 13C NMR List all the peaks in the 13C NMR and give them each a number. Write the structure of the product and label the carbons with the associated number for the peak. (The peaks from 21-25 can be...
Please answer all 3 questions
Which represents a pair of resonance structures? NH NH2 and H3C Hgc 9 CC=CH2 and 1 Hac H H H CH OH O and OOH нссон and TH H Hyc Copt н" 3 OO QUESTION 27 How many stereoisomers of 3-penten-2-ol exist? 2 3 4 0 0 QUESTION 28 What is the approximate dihedral angle between the two chlorine atoms in the diequatorial conformation of trans-1,2-dichlorocyclohexane? 0° 60° 120° 180° MacBoo
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The major product of this reaction is (4) CF NH. (B) CF (C) CF (D) no reaction CH, CH=24CH, beat The product of this rearrangement is (c) H 14 CH CHCH. (D) CH-CH2CH2 0.« *0. Which is not a reason this reaction fails to take place? (A) The C to which Cl is bonded is sp hybridized, making a shorter and stronger bond than those usually broken in substitution reactions. (B) Resonance gives the bond between...
Evaluate and investigate the
following IR Spectrum, 13C NMR Spectrum
and 1H NMR Spectrum. Identify
the most important peaks and correlate the
results as much as you can from the obtained product in
the multi-step synthesis of ethyl acetoacetate.
This is Product E from this multi-step synthesis
where Product C was identified as in the figure
below and as such, identify what product can be obtained
after the synthesis from the spectra provided. Use the template
below in analysing the...
pls answer b, g, and h
thanks
21-54 Show how you would accomplish the following syntheses. Some of these conversions may require more than one step. (a) isopentyl alcohol isopentyl acetate (banana oil) (b) 3-ethylpentanoic acid → 3-ethylpentanenitrile (c) isobutylamine → N-isobutylformamide (d) ethyl acetate → 3-methylpentan-3-ol (e) cyclohexylamine → N-cyclohexylacetamide (f) bromocyclohexane → dicyclohexylmethanol H (h) CH,OH CN O dimethyl oxalate HM N O