incorrect answers: trans-4-octene and 1-methylcyclopentene
The desired compound is not an alcohol as there is no sharp or broad peak above around 3200 cm-1. The compound is not alkene either as there are no signal for C-C double bond stretching in the range 1620 - 1680 cm-1.
The sharp peak at about 1100 cm-1 is due to C-O stretching. So, the desired compound should be dipropyl ether.
incorrect answers: trans-4-octene and 1-methylcyclopentene Which compound matches the IR spectrum? trans-4-octene 1-hexen-3-ol 1,5-hexadiene dipropyl ether...
Which compound matches the IR spectrum? 1-hexen-3-ol 1-methylcyclopentene 3-hexanol 1.5-hoxadiene cylohexane trans-4-octene dipropyl ether Which compound matches the IR spectrum? cyclohexane dipropyl ether 1-hexen-3-ol 1.5-hoxadiene 3-hexanol trans-4-octene 1-methylcyclopentene Which compound matches the IR spectrum? dipropyl ether cyclohexane 1.5-hexadiene trans-4-octene 3-hexanol 1-hexen-3-ol 1-methylcyclopentene
Which compound matches the IR spectrum? 1,5-hexadiene 1-methylcyclopentene 1-hexen-3-ol dipropyl ether cyclohexane frans-4-octene 3-hexanol
Which compound matches the IR spectrum? Dipropyl ether cyclohexane 1, 5-hexadiene 3-hexanol 1-hexen-3-ol trans-4-octene 1-methylcyclopentene
Which compound matches the IR spectrum? 1-methylcyclopentene 1-hexen-3-ol 3-hexanol cyclohexane dipropyl ether 1, 5-hexadiene trans-4-octene
27. Compound B has the following IR spectra. Choose the compound B in the above list. wavelength, micrometers 2.6 2.8 3 3.5 4 45 5 5.5 6 7 8 9 10 11 12 13 14 1516 100 E 80 E 60 c 40 ご20 0 3800 3400 3000 2600 2200 2000 1800 1600 1400 1200 1000 800 600 wavenumber, cm-1 (1.s-hexadiene, 1-methylcyclopentene, I-hexen-3-ol, dipropyl ether, trans-4-octene, cyclohexane, 3-hexanol, 0->0. ︿﹀NH2 , 27. Compound B has the following IR spectra. Choose...
What is the systematic name of compound B? (3) OH B (A) (R)-3-butyl-5-hexen-1-ol (B) (R)-4-butyl-1-hexen-6-ol (C) (S)-4-butyl-1-hexen-6-ol (D) (R)-3-allyl-1-heptanol (4) What is the major product of the following reaction? excess HC CI C (A) (B) (C) (D)
Trans-4-hexen-3-ol can be synthesized starting from acetaldehyde. One of the key reagents is ethyl grignard. 1. Synthesize ethyl grignard from acetaldehyde in the steps below using the reagents provided.
Circle which compound matches the given IR spectrum (4 pts): =O 2.6 2.8 3 3.5 4 4.5 wavelength, micrometers 5 5.5 6 7 8 9 10 11 12 13 14 1516 percent transmittance 800 600 3800 3400 3000 2600 2200 2000 1800 1600 1400 1200 1000 wavenumber, cm1 2. For the following compounds, how many signals would you expect to see in the 'H NMR spectrum (6 pts)? Сн, сн, HH
Circle which compound matches the given IR spectrum (4 pts): =O 2.6 2.8 3 3.5 4 4.5 wavelength, micrometers 5 5.5 6 7 8 9 10 11 12 13 14 1516 percent transmittance 800 600 3800 3400 3000 2600 2200 2000 1800 1600 1400 1200 1000 wavenumber, cm1 2. For the following compounds, how many signals would you expect to see in the 'H NMR spectrum (6 pts)? Сн, сн, HH
Circle which compound matches the given IR spectrum (4 pts): =O 2.6 2.8 3 3.5 4 4.5 wavelength, micrometers 5 5.5 6 7 8 9 10 11 12 13 14 1516 percent transmittance 800 600 3800 3400 3000 2600 2200 2000 1800 1600 1400 1200 1000 wavenumber, cm1 2. For the following compounds, how many signals would you expect to see in the 'H NMR spectrum (6 pts)? Сн, сн, HH