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can you please help with 1,2,3. will give high rating
1. Draw the following molecules, based...
1. Draw the following molecules, based on their IUPAC name: a) 2-hydroxy-5, 5-dimethylheptanedioic acid; b) 3-hydroxy-7-methylnonanedioic...
1. Draw the following molecules, based on their IUPAC name: a) 2-hydroxy-5, 5-dimethylheptanedioic acid; b) 3-hydroxy-7-methylnonanedioic acid 2. Give the IUPAC name for the following compounds: A) HO OH 3. Circle the name that is correct for each molecule, based on IUPAC rules. V a) 4-methylheptanoate 4-methylbutanoate b) pentyl 4-metylhexanoate c) 3-methylbutyl 4-methylhexanoate d) isobutyl 4-methylhexanoate
please answer ALL. will give a rating. thank you! Which of the following molecules can be...
please answer ALL. will give a rating. thank you!
Which of the following molecules can be oxidized to a carboxylic acid with Na2Cr2O7 in aqueous H2SO4? Select all that apply. OH OH H ول OH A B D E OD - A DE C Name the following molecule using IUPAC nomenclature. O i Name the following molecule using IUPAC nomenclature. i OH Name the following molecule using IUPAC nomenclature. H
Are these correct?? Thanks What is the IUPAC name for the following molecule? 1-Bromo-3-methylbutanecyanonitrile d. 1-Bromo-3-methylpentanenitrile...
Are these correct?? Thanks
What is the IUPAC name for the following molecule? 1-Bromo-3-methylbutanecyanonitrile d. 1-Bromo-3-methylpentanenitrile 1-Bromo-3-methylbutanenitrile 5-Bromo-3-methylpentanenitrile 5-Bromo-3-methylbutanenitrile What is the IUPAC name for the following molecule? 1-Bromo-4-cyclopentyl-3-methylbutan-2-one 5-Bromo-1 -cyclopentyl-3-methylpentan-4-one 5-Bromo-1 -cyclopentyl-3-methylpentan-4-oate 1 -Bromo-4-cyclopentyl-3-methylbutan-2-oate 4-Bromo-1 -cyclopentyl-2-methylbutan-2-one What is the IUPAC name for the following molecule? 2,4,5-Trimethylhexanol d. 2,3,5,-Trimethylhexan-2-ol 2,4,5-Trimethylhexan-2-ol 2,2,4,4-Tetramethylpentan-l-ol None of the above What is the IUPAC name for the following molecule? Isopropyl 2-methylbutyl acid 2 Isopropyl 2-methylbutyl ester Isopropyl 2-methylbutyl anhydride Methylbutyl isopropanate Isopropyl 2-methylbutanoate
please help! will give rating. thank you! Name the following molecule using IUPAC nomenclature. H Name...
please help! will give rating. thank you!
Name the following molecule using IUPAC nomenclature. H Name the following molecule using IUPAC nomenclature. o ОН Name the following molecule using IUPAC nomenclature.
VL Nomenclature: Name and draw the structures of the following organic molecules: 1) Give the IUPAC...
VL Nomenclature: Name and draw the structures of the following organic molecules: 1) Give the IUPAC name of the following compounds: CHCH2 CHCH Il III 2) Drawing Structures Methylenecyclohexane Trans-3,3-dimethyl-4-propyl-1.5-octadiene 4-methyl-12-hekadiene (3ZSE) -2,6-dimethyl-1.3.5.7-octaterne
Nomenclature: Name and draw the structures of the following organic molecules: 1) Give the IUPAC name...
Nomenclature: Name and draw the structures of the following organic molecules: 1) Give the IUPAC name of the following compounds: CHCH2 a CHCH2 II III 2) Drawing Structures Methylenecyclohexane Trans-3,3-dimethyl-4-propyl-1,5-octadiene (3Z,SE) -26-dimethyl-1,3,5,7-octatetraene 4-methyl-1,2-hexadiene
Nomenclature: Name and draw the structures of the following organic molecules: 1) Give the IUPAC name...
Nomenclature: Name and draw the structures of the following organic molecules: 1) Give the IUPAC name of the following compounds: WHICHCH2 at CHCH2 II III 2) Drawing Structures Methylenecyclohexane Trans-3,3-dimethyl-4-propyl-1,5-octadienc (3Z,SE) -2,6-dimethyl-1,3,5,7-octatetraene 4-methyl-1.2-hexadiene
4. Draw the most stable and most unstable Newman Projection for the following molecules using the...
4. Draw the most stable and most unstable Newman Projection for the following molecules using the rotation around the C3-C4 bond (use the IUPAC rules to number the chain) 5. Draw the two chair conformations for each of the following cyclohexane derivatives and then choose the conformation that is the most stable. Br BA 3 3 3 $ 2879 So ya 6. For the following compounds, identify the chiral carbons with an asterisk (*) and for those that are not...
Need help with #1! Thank you! Draw Lewis Structures for the following molecules. Give the hybridization...
Need help with #1! Thank you!
Draw Lewis Structures for the following molecules. Give the hybridization for each carbon and the approximate bond angles. a. Ethanol, CH_3CH_2OH b. Propanoic acid, CH_3CH_2COOH c. Methyl cyanide (aka acetonitrile), CH_3CN d. Ethyl propyl ether, CH_3CH_2OCH_2CH_2CH_3 e. 4-hydroxy-2-butanone, CH_3COC_H2CH_2OH f. N,N-dimethylpropamide, CH_3CH_2CON(CH_3)_2 2. Identify the functional groups: (excluding alkanes) a. Carvone (spearmint oil)
Questions 1. Draw the structure of methyl salicylate, and say what evidence indicates that methyl salicylate...
Questions 1. Draw the structure of methyl salicylate, and say what evidence indicates that methyl salicylate was formed. 2. Draw and compare the structures of acetylsalicylic acid and methyl salicylate. Circle and name the functional groups in both compounds. 3. The fragrance of apricots is due to the ester pentyl butanoate. Write the equation for the synthesis of this ester from the acid and the alcohol. 4. Give examples and names of any other compounds that contain the functional groups...
1. Draw the following molecules, based on their IUPAC name: a) 2-hydroxy-5, 5-dimethylheptanedioic acid; b) 3-hydroxy-7-methylnonanedioic acid 2. Give the IUPAC name for the following compounds: A) HO OH 3. Circle the name that is correct for each molecule, based on IUPAC rules. V a) 4-methylheptanoate 4-methylbutanoate b) pentyl 4-metylhexanoate c) 3-methylbutyl 4-methylhexanoate d) isobutyl 4-methylhexanoate
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Which of the following molecules can be oxidized to a carboxylic acid with Na2Cr2O7 in aqueous H2SO4? Select all that apply. OH OH H ول OH A B D E OD - A DE C Name the following molecule using IUPAC nomenclature. O i Name the following molecule using IUPAC nomenclature. i OH Name the following molecule using IUPAC nomenclature. H
Are these correct?? Thanks
What is the IUPAC name for the following molecule? 1-Bromo-3-methylbutanecyanonitrile d. 1-Bromo-3-methylpentanenitrile 1-Bromo-3-methylbutanenitrile 5-Bromo-3-methylpentanenitrile 5-Bromo-3-methylbutanenitrile What is the IUPAC name for the following molecule? 1-Bromo-4-cyclopentyl-3-methylbutan-2-one 5-Bromo-1 -cyclopentyl-3-methylpentan-4-one 5-Bromo-1 -cyclopentyl-3-methylpentan-4-oate 1 -Bromo-4-cyclopentyl-3-methylbutan-2-oate 4-Bromo-1 -cyclopentyl-2-methylbutan-2-one What is the IUPAC name for the following molecule? 2,4,5-Trimethylhexanol d. 2,3,5,-Trimethylhexan-2-ol 2,4,5-Trimethylhexan-2-ol 2,2,4,4-Tetramethylpentan-l-ol None of the above What is the IUPAC name for the following molecule? Isopropyl 2-methylbutyl acid 2 Isopropyl 2-methylbutyl ester Isopropyl 2-methylbutyl anhydride Methylbutyl isopropanate Isopropyl 2-methylbutanoate
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Name the following molecule using IUPAC nomenclature. H Name the following molecule using IUPAC nomenclature. o ОН Name the following molecule using IUPAC nomenclature.
VL Nomenclature: Name and draw the structures of the following organic molecules: 1) Give the IUPAC name of the following compounds: CHCH2 CHCH Il III 2) Drawing Structures Methylenecyclohexane Trans-3,3-dimethyl-4-propyl-1.5-octadiene 4-methyl-12-hekadiene (3ZSE) -2,6-dimethyl-1.3.5.7-octaterne
Nomenclature: Name and draw the structures of the following organic molecules: 1) Give the IUPAC name of the following compounds: CHCH2 a CHCH2 II III 2) Drawing Structures Methylenecyclohexane Trans-3,3-dimethyl-4-propyl-1,5-octadiene (3Z,SE) -26-dimethyl-1,3,5,7-octatetraene 4-methyl-1,2-hexadiene
Nomenclature: Name and draw the structures of the following organic molecules: 1) Give the IUPAC name of the following compounds: WHICHCH2 at CHCH2 II III 2) Drawing Structures Methylenecyclohexane Trans-3,3-dimethyl-4-propyl-1,5-octadienc (3Z,SE) -2,6-dimethyl-1,3,5,7-octatetraene 4-methyl-1.2-hexadiene
4. Draw the most stable and most unstable Newman Projection for the following molecules using the rotation around the C3-C4 bond (use the IUPAC rules to number the chain) 5. Draw the two chair conformations for each of the following cyclohexane derivatives and then choose the conformation that is the most stable. Br BA 3 3 3 $ 2879 So ya 6. For the following compounds, identify the chiral carbons with an asterisk (*) and for those that are not...
Need help with #1! Thank you!
Draw Lewis Structures for the following molecules. Give the hybridization for each carbon and the approximate bond angles. a. Ethanol, CH_3CH_2OH b. Propanoic acid, CH_3CH_2COOH c. Methyl cyanide (aka acetonitrile), CH_3CN d. Ethyl propyl ether, CH_3CH_2OCH_2CH_2CH_3 e. 4-hydroxy-2-butanone, CH_3COC_H2CH_2OH f. N,N-dimethylpropamide, CH_3CH_2CON(CH_3)_2 2. Identify the functional groups: (excluding alkanes) a. Carvone (spearmint oil)
Questions 1. Draw the structure of methyl salicylate, and say what evidence indicates that methyl salicylate was formed. 2. Draw and compare the structures of acetylsalicylic acid and methyl salicylate. Circle and name the functional groups in both compounds. 3. The fragrance of apricots is due to the ester pentyl butanoate. Write the equation for the synthesis of this ester from the acid and the alcohol. 4. Give examples and names of any other compounds that contain the functional groups...
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