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4. Convert the following structures to bond-line notation, using wedges and dashes to convey the correct...
3. (5 pts) Convert the following molecule to its zigzag representation using wedges and dashes Stick to the conventi...
3. (5 pts) Convert the following molecule to its zigzag representation using wedges and dashes Stick to the convention of having the LONGEST CARBON CHAIN remain "horizontal in your zigzag (That is, have the longest carbon chain in the plane of the paper). CH3 CI- OH I Br HO- -CH2CH3 CH3
please write out answers, thank you. Stereochemistry 5. Using dashes and wedges, Draw all the structures...
please write out answers, thank you.
Stereochemistry 5. Using dashes and wedges, Draw all the structures for the following molecules. F₃C нсусн, Он (Indicate the steochemistry) b. 6. a. Circle the stereochemistry in the following compound. Он о HO ТОН 0 OH b. What is maximum number of stereoisomers in the above compounds. Label each as diastereomer and enantiomer) c. Label each stereochemistry with Ror S configuration?
e Get Incorrect Draw a structure using wedges and dashes for the following compound: Me CI...
e Get Incorrect Draw a structure using wedges and dashes for the following compound: Me CI HO Me Cl Edit OH
convert this formula into Bond-line notation with correct bond angles. (CH3)3CCONH(CH2)2CH(CH2CH3)2
convert this formula into Bond-line notation with correct bond
angles.
(CH3)3CCONH(CH2)2CH(CH2CH3)2
Redraw (4S, 5R)-4-ethyl-5-propylnonane using wedges and dashes to show the correct stereochemistry
Redraw (4S, 5R)-4-ethyl-5-propylnonane using wedges and dashes to show the correct stereochemistry
please go into detail (about S and R configuration) as im having difficulty with this. thanks...
please go into detail (about S and R configuration) as im having
difficulty with this.
thanks
achiral 5.58 Draw bond-line structures using wedges and dashes for the following compounds: 5. rel CHE НЕОН Нонн нон (а) Сн, Et Н -ОН НО-Ен нон (b) Me Et HO- H НЕОН Нон Me (а) (c) 5.6 Me me Н но (d) Me -СІ -н Me CI- НО (e) H -н Me 5.6. 5.59 The following questions apply to the five compounds in the...
Draw the structure of each of the following compounds. Using wedges and dashes, indicate the stereochemistry....
Draw the structure of each of the following compounds. Using wedges and dashes, indicate the stereochemistry. (R)-2-Ethoxy-1, 1-dimethylcyclobutane Cyclopropyl isopropyl ether
4. Draw the following cycloalkanes as two-dimensional structures, using wedges and dashes: trans-1-bromo-2-methylcyclopentane cis--chloro-3 ethylcyclohexane trans-1,3-dimethylcyclohexane...
4. Draw the following cycloalkanes as two-dimensional structures, using wedges and dashes: trans-1-bromo-2-methylcyclopentane cis--chloro-3 ethylcyclohexane trans-1,3-dimethylcyclohexane trans-1-bromo-3 ethylcyclobutane cis-1-ethyl-4-methylcycloheptane cis-1-isopropyl-3- methylcyclopentane
10. Convert the following 3-dimensional molecule into a Fischer projection looking along the indicated line of...
10. Convert the following 3-dimensional molecule into a Fischer projection looking along the indicated line of sight. Assign an R or S designation for the absolute configuration to the chiral C. Is the molecule at the right the same or the enantiomer of the original molecule? NH2 NH2 HO CH3 OH HC H
Provide the structure for the following compounds given the IUPAC names. Use dashes and wedges to...
Provide the structure for the following compounds given the IUPAC names. Use dashes and wedges to show R and S. (2S, 4S, 6S)-2-bromo-4, 6-diethyloctane (1R, 3R, 5S)-1-bromo-3-chloro-5-isobutylcycloheptane
3. (5 pts) Convert the following molecule to its zigzag representation using wedges and dashes Stick to the convention of having the LONGEST CARBON CHAIN remain "horizontal in your zigzag (That is, have the longest carbon chain in the plane of the paper). CH3 CI- OH I Br HO- -CH2CH3 CH3
please write out answers, thank you.
Stereochemistry 5. Using dashes and wedges, Draw all the structures for the following molecules. F₃C нсусн, Он (Indicate the steochemistry) b. 6. a. Circle the stereochemistry in the following compound. Он о HO ТОН 0 OH b. What is maximum number of stereoisomers in the above compounds. Label each as diastereomer and enantiomer) c. Label each stereochemistry with Ror S configuration?
e Get Incorrect Draw a structure using wedges and dashes for the following compound: Me CI HO Me Cl Edit OH
convert this formula into Bond-line notation with correct bond
angles.
(CH3)3CCONH(CH2)2CH(CH2CH3)2
Redraw (4S, 5R)-4-ethyl-5-propylnonane using wedges and dashes to show the correct stereochemistry
please go into detail (about S and R configuration) as im having
difficulty with this.
thanks
achiral 5.58 Draw bond-line structures using wedges and dashes for the following compounds: 5. rel CHE НЕОН Нонн нон (а) Сн, Et Н -ОН НО-Ен нон (b) Me Et HO- H НЕОН Нон Me (а) (c) 5.6 Me me Н но (d) Me -СІ -н Me CI- НО (e) H -н Me 5.6. 5.59 The following questions apply to the five compounds in the...
Draw the structure of each of the following compounds. Using wedges and dashes, indicate the stereochemistry. (R)-2-Ethoxy-1, 1-dimethylcyclobutane Cyclopropyl isopropyl ether
4. Draw the following cycloalkanes as two-dimensional structures, using wedges and dashes: trans-1-bromo-2-methylcyclopentane cis--chloro-3 ethylcyclohexane trans-1,3-dimethylcyclohexane trans-1-bromo-3 ethylcyclobutane cis-1-ethyl-4-methylcycloheptane cis-1-isopropyl-3- methylcyclopentane
10. Convert the following 3-dimensional molecule into a Fischer projection looking along the indicated line of sight. Assign an R or S designation for the absolute configuration to the chiral C. Is the molecule at the right the same or the enantiomer of the original molecule? NH2 NH2 HO CH3 OH HC H
Provide the structure for the following compounds given the IUPAC names. Use dashes and wedges to show R and S. (2S, 4S, 6S)-2-bromo-4, 6-diethyloctane (1R, 3R, 5S)-1-bromo-3-chloro-5-isobutylcycloheptane
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