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![Ani] In lydohexane chair boxm, if the substituent is كنطلاصتنطعمهههلهعللها عمل کنمممهرمل مما اصع near to perpendicular this e](http://img.homeworklib.com/questions/8354aa40-0a7a-11ec-8465-199a169101e9.png?x-oss-process=image/resize,w_560)
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Identity which drawing of 1,2,3,4,5,6 hexamethylcyclohexane has all the methyl groups in adal positions, and which...
5.5. Place the methyl groups by drawing the axial and equatorial positions on the cyclohexane structure...
5.5. Place the methyl groups by drawing the axial and equatorial positions on the cyclohexane structure in the chair conformations next to the cyclohexane derivatives named below. H H CH, H CH, CH, cis-1,2-Dimethylcyclohexane H CH, trans-1,2-Dimethylcyclohexane H CH, H CH, CH, eis-1,3-Dimethylcyclohexane CH, trans-1,3-Dimethylcyclohexane H H H CH, KO HC CH, cis-1,4-Dimethylcyclohexane н,с H trans-1,4-Dimethyleyclohexane
Indicate the positions of the labeled groups in this molecule as axial or equatorial in the...
Indicate the positions of the labeled groups in this molecule as
axial or equatorial in the most stable chair conformation.
Why am I wrong????
Indicate the positions of the labeled groups in this molecule as axial or equatorial in the most stable chair conformation. a CH(CH3)2 i OH y b a CH(CH3)2 OH C CH3 cCH3 Group a: equatorial Group b: axial Group c: equatorial Group a: axial Group b: equatorial Group c: axial y An error has been detected...
N gCIL Drawing Resonance Contributors of Substituted Benzenes Identify the functional groups attached to the benzene...
N gCIL Drawing Resonance Contributors of Substituted Benzenes Identify the functional groups attached to the benzene ring as either, being electron withdrawing, electron donating, or neither Drag the appropriate structures to their respective bins. View Available Hint(s) Reset Help CHE che CH, Electron Withdrawing Groups Neither Electron Donating Groups
(2E,4E) 3-methyl-2,4 Hexadiene (2E,4Z) 3-methyl-2,4 Hexadiene (2Z, 4E) 3-methyl-2,4 Hexadiene (2Z,4Z) 3-methyl-2,4 Hexadiene the things i...
(2E,4E) 3-methyl-2,4 Hexadiene
(2E,4Z) 3-methyl-2,4 Hexadiene
(2Z, 4E) 3-methyl-2,4 Hexadiene
(2Z,4Z) 3-methyl-2,4 Hexadiene
the
things i wrote out are the compound names
Drag the appropriate structures to their respective bins. Reset Help CHL लाल CH 12041-3-methy-2.4-bemadene 2 40-3-methy-2.4hemadene 1224-3-methvi-24-hecadie
State which of these amino acids have R groups that would: a. be found in hydrophobic...
State which of these amino acids have R groups that would: a. be found in hydrophobic regions b. be found in hydrophilic regions c. form hydrogen bonds d. form salt bridges Drag the appropriate items to their respective bins. Items may be used more than once. Reset Help aspartate aspartato glycine alycine arginine arginine R groups in hydrophobic regions R groups in hydrophilic regions R groups forming hydrogen bonds Rgroups forming salt bridges
me, and m,, were written for the last electrons added to an atom. Identity which sets...
me, and m,, were written for the last electrons added to an atom. Identity which sets are vald and daily The following sets of quantum numbers, listed in the order , others by the rule or principle that is violated. Drag the appropriate items to their respective bins. View Available Hint(s) Rese Pauli violation Other violation
Determine which intermolecular forces are the dominant (strongest) forces for a pure sample of each of...
Determine which intermolecular forces are the dominant (strongest) forces for a pure sample of each of the following molecules by placing the molecules into the correct bins. Drag the appropriate molecular formula to their respective bins. View Available Hint(s) Reset Help [F] [C] [G] [CH, G] CHỌNH (CH,OH) Dispersion forces Dipol-dipolo forces Hydrogen bonding forces * Reflect in Portfolio Download Print At Alternative formats
Focusing on methyl group 4, we observe a range of variations in the spectroscopic data. Match...
Focusing on methyl group 4, we observe a range of variations in the spectroscopic data. Match the phrases in the left column to the appropriate blanks in the sentences in the right column that will help explain some of the observed spectral observations 4 4 CI CI CI 1-chloro-3- methylbutane 1-chlorobutane Drag the appropriate labels to their respective targets View Available Hint(s) Reset Help The integration at position 4 is higher in 1-chloro-3,3-dimethylbutane than in 1-chlorobutane, more methyl groups because...
plz answer all 3 parts Parta Watch the video on electron affinity and identity which of...
plz answer all 3 parts
Parta Watch the video on electron affinity and identity which of the following statements matches each reaction Check all that apply. ► View Available Hint(s) Reset Help Electron affinity is -349 Electron affinity is +349 kJ Electron affinity is -142 kJ Electron affinity is +142 kJ Electron affinity is -710 kJ Electron afinity 710 kJ Process is endothermic Process involves single electron addition a ) to a (g) 0(R) to to (g) Tole All the...
Organic Functional Groups Part A Classify each molecule as an amine, amide, or neither. Drag each...
Organic Functional Groups Part A Classify each molecule as an amine, amide, or neither. Drag each item to the appropriate bin. ► View Available Hint(s) Reset Help OH CH3CH2-N CH3CH2 CH3CH2C-NCH3 Н CH,C- N 1 CH CH CH CH COCH CH3CCH2CH3 CH,CH.CH Amine Amide Neither amine nor amide Part B Classify each molecule as an aldehyde, ketone, or neither. Drag each item to the appropriate bin. View Available Hint(s) Reset Help propanoic acid) (3 regtanone (C1,C1,0 mostry hoxancato nocara (C1;OCIĄT3...
5.5. Place the methyl groups by drawing the axial and equatorial positions on the cyclohexane structure in the chair conformations next to the cyclohexane derivatives named below. H H CH, H CH, CH, cis-1,2-Dimethylcyclohexane H CH, trans-1,2-Dimethylcyclohexane H CH, H CH, CH, eis-1,3-Dimethylcyclohexane CH, trans-1,3-Dimethylcyclohexane H H H CH, KO HC CH, cis-1,4-Dimethylcyclohexane н,с H trans-1,4-Dimethyleyclohexane
Indicate the positions of the labeled groups in this molecule as
axial or equatorial in the most stable chair conformation.
Why am I wrong????
Indicate the positions of the labeled groups in this molecule as axial or equatorial in the most stable chair conformation. a CH(CH3)2 i OH y b a CH(CH3)2 OH C CH3 cCH3 Group a: equatorial Group b: axial Group c: equatorial Group a: axial Group b: equatorial Group c: axial y An error has been detected...
N gCIL Drawing Resonance Contributors of Substituted Benzenes Identify the functional groups attached to the benzene ring as either, being electron withdrawing, electron donating, or neither Drag the appropriate structures to their respective bins. View Available Hint(s) Reset Help CHE che CH, Electron Withdrawing Groups Neither Electron Donating Groups
(2E,4E) 3-methyl-2,4 Hexadiene
(2E,4Z) 3-methyl-2,4 Hexadiene
(2Z, 4E) 3-methyl-2,4 Hexadiene
(2Z,4Z) 3-methyl-2,4 Hexadiene
the
things i wrote out are the compound names
Drag the appropriate structures to their respective bins. Reset Help CHL लाल CH 12041-3-methy-2.4-bemadene 2 40-3-methy-2.4hemadene 1224-3-methvi-24-hecadie
State which of these amino acids have R groups that would: a. be found in hydrophobic regions b. be found in hydrophilic regions c. form hydrogen bonds d. form salt bridges Drag the appropriate items to their respective bins. Items may be used more than once. Reset Help aspartate aspartato glycine alycine arginine arginine R groups in hydrophobic regions R groups in hydrophilic regions R groups forming hydrogen bonds Rgroups forming salt bridges
me, and m,, were written for the last electrons added to an atom. Identity which sets are vald and daily The following sets of quantum numbers, listed in the order , others by the rule or principle that is violated. Drag the appropriate items to their respective bins. View Available Hint(s) Rese Pauli violation Other violation
Determine which intermolecular forces are the dominant (strongest) forces for a pure sample of each of the following molecules by placing the molecules into the correct bins. Drag the appropriate molecular formula to their respective bins. View Available Hint(s) Reset Help [F] [C] [G] [CH, G] CHỌNH (CH,OH) Dispersion forces Dipol-dipolo forces Hydrogen bonding forces * Reflect in Portfolio Download Print At Alternative formats
Focusing on methyl group 4, we observe a range of variations in the spectroscopic data. Match the phrases in the left column to the appropriate blanks in the sentences in the right column that will help explain some of the observed spectral observations 4 4 CI CI CI 1-chloro-3- methylbutane 1-chlorobutane Drag the appropriate labels to their respective targets View Available Hint(s) Reset Help The integration at position 4 is higher in 1-chloro-3,3-dimethylbutane than in 1-chlorobutane, more methyl groups because...
plz answer all 3 parts
Parta Watch the video on electron affinity and identity which of the following statements matches each reaction Check all that apply. ► View Available Hint(s) Reset Help Electron affinity is -349 Electron affinity is +349 kJ Electron affinity is -142 kJ Electron affinity is +142 kJ Electron affinity is -710 kJ Electron afinity 710 kJ Process is endothermic Process involves single electron addition a ) to a (g) 0(R) to to (g) Tole All the...
Organic Functional Groups Part A Classify each molecule as an amine, amide, or neither. Drag each item to the appropriate bin. ► View Available Hint(s) Reset Help OH CH3CH2-N CH3CH2 CH3CH2C-NCH3 Н CH,C- N 1 CH CH CH CH COCH CH3CCH2CH3 CH,CH.CH Amine Amide Neither amine nor amide Part B Classify each molecule as an aldehyde, ketone, or neither. Drag each item to the appropriate bin. View Available Hint(s) Reset Help propanoic acid) (3 regtanone (C1,C1,0 mostry hoxancato nocara (C1;OCIĄT3...
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