Draw the structure of the following three isomeric amides with chemical formula C6H11NO. Amide #1: N-ethylcyclopropanecarboxamide Amide #2: (Z)-3-hexenamide Amide #3: N-methyleyclobutanecarboxamide
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Q: Primary amides have how many C-N bonds?
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Q: Draw the structure of the following three isomeric amides with chemical formula C,HNO. Amide #1:…
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Q: Which of the following molecules is an amide? B OH NH2 A) A OH B) B C) C D) D `NH2
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Q: 1) Classify the following amines as primary, secondary, tertiary or quaternary. Give the names for…
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Q: NH CH3 This amine is a amine. primary secondary quaternary O tertiary
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Q: Which compound is a primary amine with the formula C5H13N? * H2N NH II III NH2 IV V V IIl and V
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Q: Which amines cannot be prepared by reduction of an amide?
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Q: Draw the structure of the following three isomeric amides with chemical formula C6H11NO. Amide #1:…
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Q: Which amines cannot be prepared by reduction of an amide?
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Q: Which of the following is a secondary amine? NH2 NH -NH2 d) `NH2 а) b)
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Q: Which compound is a primary amine with the formula C5H13N? HN H. H2N II III N- NH2 IV V O IV II ()l…
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- Draw the structure of the following three isomeric amides with chemical formula C-H₁₁ NO. Amide #1: (Z)-N-methyl-3-pentenamide Amide #2: N-methylcyclobutanecarboxamide Amide #3: N,3-dimethyl-3-butenamide Consider E/Z stereochemistry of alkenes. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate structures with + signs from the drop-down menu. ● +*ELE ChemDoodleⓇ 4 OO. [F 11Draw the structure of the following three isomeric amides with chemical formula C,H NO. Amide #1: N-ethylcyclopropanecarboxamide Amide #2: (Z)-3-hexenamide Amide #3: N-methylcyclobutanecarboxamide • Consider E/Z stereochemistry of alkenes. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Separate structures with + signs from the drop-down menu. opy aste ChemDoodle (Provious Next Email Instructor Save aDraw the structure of the following three isomeric amides with chemical formula C,H|NO. Amide #1: (E)-N,N-dimethyl-2-butenamide Amide #2: (Z)-N-methyl-3-pentenamide Amide #3: (Z)-3-hexenamide Consider E/Z stereochemistry of alkenes. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Separate structures with + signs from the drop-down menu. ору aste ChemDoodle Previous Next Email Instructor Save and Exit
- Provide the systematic name for each of the following isomeric amides with the chemical formula C6H₁1 NO. (Be sure to indicate double bond stereochemistry using (E)/(Z) notation. Indicate stereochemistry in rings with the terms cis or trans. It is not necessary to use italics in writing compound names.) ball & stick + labels N-methylpent-4-enamide An error has been detected in your answer. Check for typos, miscalculations etc. before submitting your answer. ball & stick - + labels N, 3-dimethylbut-3-enamide ball & stick + labels (2Z)-2-methylpent-2-enamideThis question has multiple parts. Work all the parts to get the most points. Answer true or false. a In the IUPAC system, primary aliphatic amines are named as alkylamines. true false b The IUPAC name of CH3 CH₂ CH₂ CH₂ CH₂NH2 is 1-pentanamine. true false C 3-Pentanamine is chiral and shows enantiomerism. true false dN-Ethylpropylamine is a 2º aromatic amine. true false Submit Answer Try Another Version 3 item attempts remaining16-17 Propylamine (bp 48°C), ethylmethylamine (bp 37°C), and trimethylamine (bp 3°C) are constitutional isomers with the molecular formula C3HgN. Account for the fact that trimethylamine has the lowest boiling point of the three and propylamine has the highest.
- 11.27: Tell which is the stronger base and why? Aniline or p-cyanoaniline b) aniline or diphenylamine WH₂ |ال 11.30: Place the following substances, which have nearly identical formula weights, in order of increasing boiling point? 1-aminobutane, 1-butanol, methyl propyl ether, pentaneEstrogens are female sex hormones, the most potent of which is B-estradiol. OH AYA Но B-Estradiol In recent years, chemists have focused on designing and synthesizing molecules that bind to estrogen receptors. One target of this research has been nonsteroidal estrogen antagonists, compounds that interact with estrogen receptors and block the effects of both endogenous and exogenous estrogens. A feature common to one type of nonste- roidal estrogen antagonist is the presence of a 1,2-diphenylethylene with one of the benzene rings bearing a dialkylaminoethoxyl substituent. The first nonsteroidal estrogen antagonist of this type to achieve clinical importance was tamoxifen, now an important drug in the treatment of breast cancer. Tamoxifen has the Z configuration shown here. NMeg A B NMeg ? ОН Tamoxifen Propose reagents for the conversion of A to tamoxifen. Note: The final step in this synthesis gives a mixture of E and Z isomers.Provide the systematic name for each of the following isomeric amides with the chemical formula C,HNO. (Be sure to indicate double bond stereochemistry using (E)/(Z) notation. Indicate stereochemistry in rings with the terms cis or trans. It is not necessary to use italics in writing compound names.) H 旧 C ball & stick labels ball & stick labels ball & stick labels
- Which type of compound typically give 3 peaks ("bands") between approx. 1500-1600 cm in an IR spectrum? Select one: Carbonates Esters Alkaloids Aromatic compoundsEistrogens are female sex hormones, the most potent of which is B-estradiol. OH H,C но B-Estradiol In recent years, chemists have focused on designing and synthesizing molecules that bind to estrogen receptors. One target of this research has been nonsteroidal estrogen antagonists, compounds that interact with estrogen receptors and block the effects of both endogenous and exogenous estrogens. A feature common to one type of nonste- roidal estrogen antagonist is the presence of a 1,2-diphenylethylene with one of the benzene rings bearing a dialkylaminoethoxyl substituent. The first nonsteroidal estrogen antagonist of this type to achieve clinical importance was tamoxifen, now an important drug in the treatment of breast cancer. Tamoxifen has the Z configuration shown here. но NMe, NMeg ? B NMeg ? "NMe, ОН Tamoxifen Propose reagents for the conversion of A to tamoxifen. Note: The final step in this synthesis gives a mixture of E and Z isomers.Provide the systematic name for each of the following isomeric amides with the chemical formula C₂H₁1 NO. (Be sure to indicate double bond stereochemistry using (E)/(Z) notation. Indicate stereochemistry in rings with the terms cis or trans. It is not necessary to use italics in writing compound names.) ball & stick V labels ball & stick- + labels ball & stick v labels