Draw the following condensed (or skeletal if cyclo) structural diagrams p-chlorobenzaldehyde (skeletal is acceptable) diethyl ketone N,N-dimethyl-2-propanamine
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Draw the following condensed (or skeletal if cyclo) structural diagrams
p-chlorobenzaldehyde (skeletal is acceptable)
diethyl
N,N-dimethyl-2-propanamine
3-methyl-5-chloroheptanal
3-methoxyhexane
methyl pentanoate
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Solved in 3 steps with 3 images
- Which of (a)-(d) is the correct IUPAC name of the following compound? * HO O 3-methyl-1-phenyl-1-pentanol ○ 3-methyl-5-phenyl-5-pentanol ○ 3-methyl-1-benzene-1-pentanol O 1-phenyl-1-hexanolDraw the following functional groups. 4-ethyl-5-isopropyl-2,3-dimethyl-2,4-nonadien-6-ynedial4-hydroxy-3-methoxycyclohexane-1-carboxylic acidWhat reaction conditions are needed to convert (R)-2-ethyl-2-methyloxirane to (S)-2- methylbutane-1,2-diol ?
- What is the systematic IUPAC name for the following Organic compound? Br CI 1-bromo-2-chloro-4-ethoxybenzene O 1-bromo-6-chloro-4-cthoxybenzene O 1-cthoxy-3-chloro-4-bromobenzene O1-ethoxy-4-bromo-5-chlorobenzene 1-chloro-2-bromo-5-cthoxybenzene 1-chloro-3-ethoxy-6-bromobenzeneThe IUPAC name of the compound H- is (a) 5-formylhex-2-en-3-one (b) 5-methyl-4-oxohex-2-en-5-al (c) 3-keto-2-methylhex-5-enal (d) 3-keto-2-methylhex-4-enal ( The correct statement regarding electrophile is (a) electrophile is a negatively charged species and can form a bond by accepting a pair of electrons from another electrophile (b) electrophiles are generally neutral species and can form a bond by accepting a pair of electrons from a nucleophile (c) electrophile can be either neutral or ar positively charged species and can form a bond by accepting a pair of electrons from a nucleophile (d) electrophile is a negatively charged species and can form a bond by accepting a pair of electrons from a nucleophile.. Which among the given molecules can exhibit tautomerism? Ph Ph I II III (a) III only (c) Both I and II (b) Both I and III (d) Both II and III 1) Which of the following biphenyls is optically active?What is the IUPAC name of the following compound? * CEN H2 | H2 H3C-CEC -С—с—с—ОН H3C 2-Methyl-2-hydroxymethylhex-4-yne nitrile 2-Cyano-2-methylhex-4-yne-ol 2-Hydroxymethyl-2-methylhex-4-yne nitrile 1-Cyano-2-hydroxymethyl-2-methylhex-4- yne
- < Provide the correct IUPAC name for the compound shown here. u 1- H3C Question 22 of 25 3- sec- oic 5- tert- 2- 4- CH3 iso di cyclo tri pent prop eth J but meth hex 6- acid aldehyde Submit +Draw the line structure of the following compound. (2E,5R,7Z)-3-benzyl-8-bromo-4-(1-chloroethyl)-N-ethyl-7-methoxy-N,9-dimethyl-2,7-decadien-5-amineCitronellol ((3R)-3,7-dimethyloct-6-en-1-ol, C10H20O) is an organic fragrance found in the oil extracted from lemon grass. a) Name the two functional groups present in the molecule. b) When a few drops of bromine dissolved in hexane is added to a sample of citronellol the brown colour of the bromine rapidly disappears. i. What type of chemical reaction has occurred? ii. Draw the structure of the product formed. iii. Name the product. c) The product formed when citronellol is heated with a mixture of potassium dichromate and sulfuric acid gives a yellow/orange precipitate when shaken with Brady’s reagent (2,4-dinitrophenylhydrazine). It also shows a positive result with Fehling’s solution. i. What type of chemical reaction has occurred ? ii. What type of functional group is present in the product? d) Explain the type of stereoisomerism which may occur in citronellol.
- 30. Name the following compound using systematic IUPAC nomenclature. Br (A) 3-bromo-2-methylheptanone (B) 4-bromo-5-methylheptanone (C) 5-bromo-6-methyl-2-heptanone (D) 4-bromo-5-methylheptanalName: Organic Chemistry Nomenclature Project Carboxylic Acids CH, CH, CH OH pentanoic acid H,C- H;C. OH H3C- CH3 CH. 2,5-dimethyl-3-heptenoic acid 4-cyclopropyl-2-nitro-3-butynoic acid он CH 4 methylbut-2-enoic acid OH butadioic acidName: Organic Chemistry Nomenclature Project Esters CH3 H,C- propyl butanoate phenyl hexanoate dichloromethyl-2-ethoxypropanoate Br CH3 H,C CH3 methyl propanotate CH3 H3C CH3 2- nitrohexyl ethanoate