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22 Select the correct row of names that correctly corresponds to the structures above them O...
20) Which of the following compounds gives an infrared spectrom which peaks a 3000-3500 cmt and \700 cm ir он с? А? D? В? Q) a compound with the molecular formular C3 Hia HN MR Spectrum Singlet gave the following 81.0 (12H). The structure of the compound is СНа снасна сносна © сHз сHсна сіз сH3 CH3 СН3 CH3CH CH CH2 ② CH₃CCH3 СНа сH3 1 сна 22 Select the correct row of names that correctly corresponds to the structures...
1-10 Name: Total 100 pts (25X4 pts) 1) Which of the following is the best name for the following compound? A) 1,2-Dichloropentanal )1-Chloro-1-butanecarbonyl chloride C) 2-Chloropentanoyl D) 1-Chloropentanoyl chloride 2) Which of the following is the best name for the following compound? 0 a) tsobutyl ethanoate d) Ethoxy isobutyl ketone b) Ethyl isopropanoate c) 3-methylbutyl ethanoate e) Ethyl 3-methylbutanoate 3) Which compound would have highest pKa? E) D) B) A) 4) Which of the following would be the strongest acid?...
1. Give IUPAC names for the following compounds: O H.C =CH-C-NH2 H,00 H.CO 2. Draw structures corresponding to each of the given names. Ethyl 4-aminobenzoate acetic formic anhydride 3. What is the order of decreasing reactivity towards nucleophilic acyl substitution for the carboxylic acid derivatives? (most reactive first) H,C-4-0--CHHC-2-N(CH) Hc--OCH, (CH),CH----OCH,
21) Consider the following structures I-IV. Circle the two species that represent resor sonance structures H. O: :0: H .H N. N: 22) Circle the base and the conjugate base in the following reaction но CH,COO CH COOH HO IV ш II Chapter 3 particular molecule? 23) Why do z bonds confer reactivity on a A) Because n bonds are diffficult to break in chemical reactions. B) Because z bonds make a molecule an acid. C) Because z bonds are...
Give the names of each organic families shown. (Careful with spelling) My answers are partially correct please tell me all the right anaswers Give the names of each organic families shown. Careful with spelling) O=O solo con modulelos.com.br CH,CH,CH; CH,CH,CH; CH,CH,CH; | CHỊCH C-O-C- CHỊCH, CHỊCH - NH Он Br ос,н. Compound I is a(n) amide Compound II is a(n) carboxylic acid Compound III is a(n) aldehyde Compound IV is a(n) alcohol Compound V is a(n) ester Submit >
Formation and Hydrolysis of Amides Identify the products by dragging the appropriate labels to their respective targets. Part A When acyl halides (R-COX) or acid anhydrides (R-OC-O-CO-R) react with primary amines (R-NH2) or secondary amines (R2 NH), the reaction yields an amide R-C-NR2 where R may be an alkyl group or hydrogen atom For example, propanoyl chloride |l reacts with ethanamine (CH3 CH2NH2) to form The IUPAC name for CH3 CH2C-Cl CH3 CH2C-NHCH2CHa the product is N-ethyl propanamide, as it...
3) Write the names of the molecules whose explicit structures are given below, according to the naming system. Write the open structures of the named compounds NH он a) CH3 соон NO2 b) ON -COOH -NOZ d) e) h) f) 2-Naphthoic acid g) 2,10-dimetilantras anisole i) o-cresol j) 3-aminopyridine 4) Using all the benzene as given in the reaction below, show all the steps necessary to synthesize the target compound, o-nitroaniline. Indicate what is the appropriate reagent in each step...
1) Name the following carboxylic acids (use both IUPAC and common names): ОН ОН (b) (c) ОН ОН (d) Br ОН ОН NH2 2) Draw the condensed and line structures for the following compounds (a) 3,4-dimethylhexanoic acid (b) Phenylacetic acid (c) 3,4-dinitrobenzoic acid (d) 2,2,3-triflurobutanoic acid (e) 3-hydroxybutanoic acid (1) o-hydroxybenzoic acid (g) a-aminopropionic acid 3) Name the following dicarboxylic acids (use both IUPAC and common names) Он (а) НО ОН НО. (b) он ОН ОН (d) ОН он ОН...
When acyl halides (R?COX) or acid anhydrides (R?OC?O?CO?R) react with primary amines (R?NH2) or secondary amines (R2NH), the reaction yields an amide: O || R?C?NR2 where R may be an alkyl group or hydrogen atom. For example, propanoyl chloride ( O ||CH3CH2C?Cl) reacts with ethanamine (CH3CH2NH2) to form (O || CH3CH2C?NHCH2CH3). The IUPAC name for the product isN-ethyl propanamide, as it is formed from ethanamine and propanoyl chloride. Match the names of the products for the following reactions. Identify the products by dragging the appropriate labels...
12) Draw a line angle formula (you do not need to redraw f g, k, 1 n, & o), showing all the bonds within each functional group, and then classify the compounds. The possible classifications are as follows: Alcohol Ketone Carboxylic acid Ether Aldehyde Nitrile Alkyne Ester Amide Acid halide Anhydride Alkene Amine (24 pts) (a) CH3CH2CHO (b) CH3CH2CH(OH)CH; (C) CH3COCH2CH3 (d) CH3CH2OCHCH; (e) (CH3)3CCH2CH2COOH CHC(CH3)2 -CCH N-CH (k wachance for clear N-CHZ C-CH (m)(CH3CH2)3CCH COCI