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In a Word document, answer the questions below: 1. The chromophore of GFP is what gives...
1. The chromophore of GFP is what gives off the bright light. In the structure shown...
1. The chromophore of GFP is what gives off the bright light. In the structure shown belovw, circle 1 amide, 1 amine, 1 carboxylic acid, and 1 alcohol CH E H CH . In the structure shown above, (a) how many amides are there? (b) amines? (c) carboxylic acids (d) and phenols?
please answer b *PLEASE DO NOT FORGET THE EXPLANATION* b. Circle the most likely structure that...
please answer b
*PLEASE DO NOT FORGET THE EXPLANATION*
b. Circle the most likely structure that corresponds to the IR spectrum: Spectrum: Explanation (be specific): Infrared Absorption Bands Frequency (cm ) Type of Vibration Intensity C-H Alkanes -CH -CH2- Alkenes (stretch) (bend) (bend) (stretch) (out-of-plane bend) (stretch) (out-of-plane bend) (stretch) Aromatics 3000-2850 1450 and 1375 1465 3100-3000 1000-650 3150-3050 900-690 ca. 3300 2900-2800 2800-2700 Alkyne Aldehyde O-H Alcohol, phenols Free H-bonded Carboxylic acids Primary and secondary amines and amides (stretch)...
please answer C and PLEASE do not forget the explanation C. Circle the most likely structure...
please answer C and PLEASE do not forget the
explanation
C. Circle the most likely structure that corresponds to the IR spectrum: OH OH Explanation (be specific): Spectrum: ARVENUHERIA Infrared Absorption Bands Frequency (cm ) Intensity Type of Vibration C-H Alkanes -CH -CH- Alkenes (stretch) (bend) (bend) (stretch) (out-of-plane bend) (stretch) (out-of-plane bend) (stretch) 3000-2850 1450 and 1375 1465 3100-3000 1000 650 3150 3050 900-690 ca. 3300 2900-2800 2800-2700 Aromatics Alkyne Aldehyde 0-н 3650-3600 3400-3200 3400-2400 Alcohol, phenols Free H-bonded...
3) Four of the compounds below contain carbonyl functional groups. a). What stretching frequency will they...
3) Four of the compounds below contain carbonyl
functional groups.
a). What stretching frequency will they have in common? Name the
bond and typical cm^-1
b). Are there variations in the stretching frequency that you named
above for the different carbonyl functional groups? If so,
what?
Infrared Absorption Bands Frequency (cm ) Type of Vibration Intensity C-H Alkanes -CH --CH, Alkenes (stretch) (bend) (bend) (stretch) (out-of-plane bend) (stretch) (out-of-plane bend) (stretch) 3000-2850 1450 and 1375 1465 3100-3000 1000-650 3150-3050 900-690...
INFRARED SPECTROSCOPY 1. Circle AND label the functional groups in each molecule. Then predict the signal(s)...
INFRARED SPECTROSCOPY
1. Circle AND label the functional groups in
each molecule. Then predict the signal(s) that
would result from each functional group in the IR.
PLEASE ANSWER (C) and (D please follow the directions
and write neatly
Но, ес -CEC-H Infrared Absorption Bands Type of Vibration Frequency (cm21) Intensity C-H Alkanes CH CH- Alkenes (stretch) (bend) (bend) (stretch) (out-of-plane bend) (stretch) (out-of-plane bend) (stretch) Aromatics 3000-2850 1450 and 1375 1465 3100-3000 1000-650 3150-3050 900-690 ca. 3300 2900-2800 2800-2700 Alkyne...
Please answer all questions 6) Identify the correct IUPAC systematic name for the structure below. who...
Please answer all questions
6) Identify the correct IUPAC systematic name for the structure below. who -CH H A) N-methyl-2-ethyl-5-methyloctanamide B) 6,N-dimethylnonane-3-carboxamide C) 5,N-dimethyl-2-ethyloctanamide D) 2-ethyl-5,N-dimethyloctanamide 7) Which of the following is the most reactive carboxylic acid derivative? A) ester B) anhydride C) nitrile D) acid chloride E) amide 8) Identify the carboxylic acid derivative/s in the structure of Lactimidomycin. HN OH O A) Ester B) Anhydride C) Nitrile D) Imine 9) Arrange the carboxylic acid derivatives below in order...
POSTLAB QUESTIONS Name Date Instructor Organic Models and Nomenclature 1. Name the following compounds using the...
POSTLAB QUESTIONS Name Date Instructor Organic Models and Nomenclature 1. Name the following compounds using the IUPAC nomenclature system: a. CH CH.CH,CH,CH, Peptone b. CH CH CHCHCH, I methu Pentare CH, CH, c. CH CH CCH CH 2. Draw the constitutional (structural) isomers of C,H, 3. Draw the structure of trans-2-butene, and then sketch the product that would result if this compound reacted with bromine, Br, Postlab Questions: Organic Models and Nomencla 4. Circle the functional groups on the molecules...
____ 1. The diagram below represents serine, a polar, uncharged amino acid. Which functional group gives...
____ 1. The diagram below represents serine, a polar, uncharged
amino acid. Which functional group gives serine its
distinct property?
a. H3
b. CH2OH
c. –H
d. COO–
____ 2. The monomers shown below are monomers for which of the
following natural polymers?
a. polysaccharides
b. plastics
c. DNA
d. proteins
____ 3. Which of the following processes illustrates the production
of a protein?
a. specific code for amino acids --> amino acid chain -->
gene --> DNA --> specific...
Please show any work or explanation and help with filling out the data table. I appreciate...
Please show any work or explanation and help with
filling out the data table. I appreciate it very much. Thank
you!
5. (Opts) Propose opts) Propose a reasonable to heterostom for the organic molecule that gave rise to the spectra below. Complete the me poctra below. Complete the datablas below related to the structure that you've identified Mass Spectrum 100 Relative Intensity 10 20 30 40 50 70 80 90 60 m/z 100 110 IR Spectrum 028 1936.93 13C NMR...
which of the above 8 terpenes does the IR spectrum belongs to ? determine the peaks...
which of the above 8 terpenes does the IR spectrum
belongs to ?
determine the peaks that belongs to the terpene.
attached are reference table for finding peaks .
U right scandidate terpenes narrone Citral litronellol p-upmene Myreene geraniol linenene Menthone Transance 4000 101 - Wed Oct 15 703 322019 GMT-0001 3500 3000 2964.0B 304704 3D08.40 2919.65 205448 2500 2000 1715.80 1645.25 1622 07 159331 1576 51 1495 54 1449.04 1376.494 133870 126369 115592 109716 980 65 955.96 914 BBB...
1. The chromophore of GFP is what gives off the bright light. In the structure shown belovw, circle 1 amide, 1 amine, 1 carboxylic acid, and 1 alcohol CH E H CH . In the structure shown above, (a) how many amides are there? (b) amines? (c) carboxylic acids (d) and phenols?
please answer b
*PLEASE DO NOT FORGET THE EXPLANATION*
b. Circle the most likely structure that corresponds to the IR spectrum: Spectrum: Explanation (be specific): Infrared Absorption Bands Frequency (cm ) Type of Vibration Intensity C-H Alkanes -CH -CH2- Alkenes (stretch) (bend) (bend) (stretch) (out-of-plane bend) (stretch) (out-of-plane bend) (stretch) Aromatics 3000-2850 1450 and 1375 1465 3100-3000 1000-650 3150-3050 900-690 ca. 3300 2900-2800 2800-2700 Alkyne Aldehyde O-H Alcohol, phenols Free H-bonded Carboxylic acids Primary and secondary amines and amides (stretch)...
please answer C and PLEASE do not forget the
explanation
C. Circle the most likely structure that corresponds to the IR spectrum: OH OH Explanation (be specific): Spectrum: ARVENUHERIA Infrared Absorption Bands Frequency (cm ) Intensity Type of Vibration C-H Alkanes -CH -CH- Alkenes (stretch) (bend) (bend) (stretch) (out-of-plane bend) (stretch) (out-of-plane bend) (stretch) 3000-2850 1450 and 1375 1465 3100-3000 1000 650 3150 3050 900-690 ca. 3300 2900-2800 2800-2700 Aromatics Alkyne Aldehyde 0-н 3650-3600 3400-3200 3400-2400 Alcohol, phenols Free H-bonded...
3) Four of the compounds below contain carbonyl
functional groups.
a). What stretching frequency will they have in common? Name the
bond and typical cm^-1
b). Are there variations in the stretching frequency that you named
above for the different carbonyl functional groups? If so,
what?
Infrared Absorption Bands Frequency (cm ) Type of Vibration Intensity C-H Alkanes -CH --CH, Alkenes (stretch) (bend) (bend) (stretch) (out-of-plane bend) (stretch) (out-of-plane bend) (stretch) 3000-2850 1450 and 1375 1465 3100-3000 1000-650 3150-3050 900-690...
INFRARED SPECTROSCOPY
1. Circle AND label the functional groups in
each molecule. Then predict the signal(s) that
would result from each functional group in the IR.
PLEASE ANSWER (C) and (D please follow the directions
and write neatly
Но, ес -CEC-H Infrared Absorption Bands Type of Vibration Frequency (cm21) Intensity C-H Alkanes CH CH- Alkenes (stretch) (bend) (bend) (stretch) (out-of-plane bend) (stretch) (out-of-plane bend) (stretch) Aromatics 3000-2850 1450 and 1375 1465 3100-3000 1000-650 3150-3050 900-690 ca. 3300 2900-2800 2800-2700 Alkyne...
Please answer all questions
6) Identify the correct IUPAC systematic name for the structure below. who -CH H A) N-methyl-2-ethyl-5-methyloctanamide B) 6,N-dimethylnonane-3-carboxamide C) 5,N-dimethyl-2-ethyloctanamide D) 2-ethyl-5,N-dimethyloctanamide 7) Which of the following is the most reactive carboxylic acid derivative? A) ester B) anhydride C) nitrile D) acid chloride E) amide 8) Identify the carboxylic acid derivative/s in the structure of Lactimidomycin. HN OH O A) Ester B) Anhydride C) Nitrile D) Imine 9) Arrange the carboxylic acid derivatives below in order...
POSTLAB QUESTIONS Name Date Instructor Organic Models and Nomenclature 1. Name the following compounds using the IUPAC nomenclature system: a. CH CH.CH,CH,CH, Peptone b. CH CH CHCHCH, I methu Pentare CH, CH, c. CH CH CCH CH 2. Draw the constitutional (structural) isomers of C,H, 3. Draw the structure of trans-2-butene, and then sketch the product that would result if this compound reacted with bromine, Br, Postlab Questions: Organic Models and Nomencla 4. Circle the functional groups on the molecules...
____ 1. The diagram below represents serine, a polar, uncharged
amino acid. Which functional group gives serine its
distinct property?
a. H3
b. CH2OH
c. –H
d. COO–
____ 2. The monomers shown below are monomers for which of the
following natural polymers?
a. polysaccharides
b. plastics
c. DNA
d. proteins
____ 3. Which of the following processes illustrates the production
of a protein?
a. specific code for amino acids --> amino acid chain -->
gene --> DNA --> specific...
Please show any work or explanation and help with
filling out the data table. I appreciate it very much. Thank
you!
5. (Opts) Propose opts) Propose a reasonable to heterostom for the organic molecule that gave rise to the spectra below. Complete the me poctra below. Complete the datablas below related to the structure that you've identified Mass Spectrum 100 Relative Intensity 10 20 30 40 50 70 80 90 60 m/z 100 110 IR Spectrum 028 1936.93 13C NMR...
which of the above 8 terpenes does the IR spectrum
belongs to ?
determine the peaks that belongs to the terpene.
attached are reference table for finding peaks .
U right scandidate terpenes narrone Citral litronellol p-upmene Myreene geraniol linenene Menthone Transance 4000 101 - Wed Oct 15 703 322019 GMT-0001 3500 3000 2964.0B 304704 3D08.40 2919.65 205448 2500 2000 1715.80 1645.25 1622 07 159331 1576 51 1495 54 1449.04 1376.494 133870 126369 115592 109716 980 65 955.96 914 BBB...
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