1) Name the following compound: 2) Name the following compound: Br 3) Draw the structure of...
5. Draw a structure for and name a compound that is consistent with compound that is consistent with the following MS. abundance 73 M 80 90 100 110 120 130 140 150 160 10 20 30 40 50 60 70 m/z Question 5: Structure and name: Mass Spectrum (include the molecular ion) Observed Fragment & MW Expected MW Fragmentation type Explanation:
1. Give the correct name for each compound. 2. Determine the degree of unsaturation for the molecular formula, C.H.BrCl. Draw and name at least five isomers for the above molecular formula. 3. Draw a structure for each compound. (a) (E)-2-chloro-2-hexene (b) (3,6Z)-1,3,6-octatriene (c) trans-3-methylhept-3-ene 4. Predict the elimination product(s) formed by debromination of the following compound with iodide ion in acetone. Include stereochemistry, and give a correct name for the product. B -CH₃ "Br + Acetone r A CH₂ 5....
Name or draw the following Prepare the following using reagents or conditions necessary. Name: CHM 2210 Exam 1 Fall 2019 1. Name or draw the following (3 pts each, 18 pts) a. Trans-1,3-Difluorocyclopentane b. (Z)-5-Ethyl-4-isopropyl-1,5-heptadiene c. (3,5E,7Z)-5,7-Diethyl-4-methyl-3,5,7-decatriene that - - hexene d. propyl 2- Bromo-4 propyl t-hexene 3.5-octadiene E e. $23-chloro-6-methyl-3.5-octadiene Me e 3-Ethyl-2-methyl-4-nitro-l-nonene ON nitro ОН Br Br - он All/Br Markou КОН - H₂O H3Rou 2sche + ALI ОН ОН ВСоон BH3 THE ноо оң Arcool-1
1. Name the following compound NO2 POINTS: 1 2. Name the following compound Br NH2 POINTS 1 3. Name the following compound CI OH POINTS: 1 4. Name the following compound
1. Draw the structures of: a) (Z) 2-iodo-3-methyl-2-heptene b) cis non-3-en-5 yne Give the IUPAC name of the following compounds, including steochemistry. a) F CH2CH2Br CH3CE 2. a) Draw the most stable chair conformation of cis 1,3-difluorocyclohexane. b) Draw a Newman projection of 2-iodo-3-methylpentane looking down the 3. Compound X has the formula CoHB2Br4. Compound X reacts with excess H2/Pd to give CATHa6Bra. How many does compound X have? Show how you got your answer. rings 4. For each pair...
1.) Name the following compounds including stereochemistry. + Br 2.) Assign configurations to each of the chiral centers and circle the stereochemical relationship of the two compounds shown below in Fischer notation? CH3 C2H5 Br- H CH HCI Brt CzH5 A) enantiomers. B) diastereomers - C) constitutional isomers- D) cis/trans - isomers E) meso - same structure CH3 3.) Draw the structure of the meso form of 1,3-dichlorocyclopentane. Take particular care to indicate three-dimensional stereochemical detail properly. -
Provide the appropriate IUPAC name for the following structure. Include E or Z notation. Br 5 ク
1. provide the IUPAC name and draw for the following compound . (CH3)3CCCH(CH3)2 2. draw an acceptable structure for 3-hexyne. 3. draw the structure for the following compound. (3Z,5E) 4-methyl-3,5-nonadiene
Which of the following is the correct structure of Compound A? 1) Br, CH C 2) 2.6 eq. NaNH. NH3の 3) H2. Lindlar's catalyst Compound A IV. Br V. OC. Il O D.I O E. IV
1 a) For each of the following compounds, give the IUPAC suffix and the chain length as demonstrated for the example. Compound IUPAC Chain Compound IUPAC Chain suffix length suffix length OH -ol 4 OH alcohol OH O w nii CHE Br i Ulo OH N(CH3)2 b) Match each of the following structures with the proper IUPAC name. Note that there are more names than structures (not all names will be used). CH3 Br CI Br Br CH, a) 2,4-dimethyl-1,3-cyclopentadiene...