. Name the molecules below, using stereochemical labels (cis/trans and E/Z) and regiochemical (meta-, ortho-, or...
5. Name the following compound using the ortho (o), meta (m) or para (p) designation. HO .CI Enter the name of the compound here SubmitX
2. Compound A reacts with E+ to form the ortho and meta intermediates shown below. ENN Orice om contato M1 M2 The least stable intermediate is ___, which tells me the CN group is a director. Check two (2) boxes. N 01 (blank 1) O O 02 (blank 1) 03 (blank 1) 04 (blank 1) M1 (blank 1) M2 (blank 1) M3 (blank 1) M4 (blank 1) O ortho, para (blank 2) O meta (blank 2)
3. a) Decide whether these alkenes should be described as E or Z. Only write the full name if indicated you should. (also give full name) H Br b) Decide whether these arenes should be described as ortho, meta or para. pelom aid Br Br но. CI OH 4. a) Why is it unnecessary to use the cis/trans or E/Z labels label to describe the double bond geometry in a cyclohexene? oranunsbg2 sb b) Rank these alkenes in order of...
In the box below, enter the name of this compound Use R/S, E/Z, cis/trans designations where necessary. он TTTT Paragraph o Arial (126) %DOQEEEE93 TT. 2 . E T... - -
2) Name the following using cis/trans or E/Z nomenclature when necessary. O CH,Br =C CH HOCH CH CH C1 СІН, CH,CH CH CH CH CH3 C=C HAC CHCH,CI
Correctly name these compounds as cis (Z) or trans (E) isomers, using the CIP rules:
Please, state the IUPAC name and give trans/cis (E and Z) if
needed. Thank you.
1. Determine the appropriate IUPAC name for the following compounds from their line- angle structures. (6 points)
1. Name these compounds according to the IUPAC system. Include stereochemistry (cis/trans, E/Z) where shown. 5,7-dimethyl
1. Name these compounds according to the IUPAC system Include stereochemistry (cis/trans, E/Z) where shown. 4 Write "most" under the alkene which is most stable. Write "least" under the alkene which is least stable. 3. Write in the product of this reaction: HBO HBr
1)- Give the correct names for the structures drawn (i.e. A-E) or draw the structure for each of the names given (i.e., F) for the compounds below, and use the E/Z, cis/trans, equatorial/axial, R/S labeling when appropriate (Choose 4 overall which include A and E) он O2N NO2 CN NO2 Br Common Name (CH,)-СОНСОН(CH3)2 Common Name 4-Carbomethoxy-5-formyl-2-hydroxybenzenesulfonic acicd
1)- Give the correct names for the structures drawn (i.e. A-E) or draw the structure for each of the names given (i.e.,...