{"id":7894,"date":"2021-01-04T04:03:36","date_gmt":"2021-01-04T04:03:36","guid":{"rendered":"https:\/\/courses.lumenlearning.com\/chemistryformajors\/?post_type=chapter&p=7894"},"modified":"2021-01-04T04:03:36","modified_gmt":"2021-01-04T04:03:36","slug":"assignment-organic-chemistry-practice","status":"publish","type":"chapter","link":"https:\/\/courses.lumenlearning.com\/chemistryformajors\/chapter\/assignment-organic-chemistry-practice\/","title":{"raw":"Assignment: Organic Chemistry Practice","rendered":"Assignment: Organic Chemistry Practice"},"content":{"raw":"
    \r\n \t
  1. Write the chemical formula, and Lewis structure for each of the following hydrocarbons:<\/li>\r\n<\/ol>\r\n(a) pentane\r\n\r\n(b) 3-ethylhexane\r\n\r\n(c) cis-4-hepten-1-ol\r\n\r\n(d) 4-methyl-1-hexene\r\n\r\n(e) 2-heptyne\r\n\r\n(f) 3,4-dimethyl-1-octyne\r\n
      \r\n \t
    1. Describe the difference between a saturated and unsaturated hydrocarbon. What would the hybridization be at the crucial carbons in each kind of molecule?<\/li>\r\n \t
    2. Write a condensed structural formula, such as CH3CH3, and describe the molecular geometry at each carbon atom.<\/li>\r\n<\/ol>\r\n(a) propene\r\n\r\n(b) 1-butanol\r\n\r\n(c) ethyl propyl ether\r\n\r\n(d) cis-4-bromo-2-heptene\r\n\r\n(e) 2,2,3-trimethylhexane\r\n\r\n(f) formaldehyde\r\n
        \r\n \t
      1. Write out the resonance structures for the acetate ion.<\/li>\r\n \t
      2. Complete the activity linked here<\/a> (https:\/\/www2.chemistry.msu.edu\/faculty\/reusch\/virttxtjml\/questions\/General\/match10.htm<\/a>) doing structure matching to formulas. Come back and type the letter answers in the order they appeared (Left to right).<\/li>\r\n \t
      3. Complete the activity linked here<\/a>. (https:\/\/www2.chemistry.msu.edu\/faculty\/reusch\/virttxtjml\/questions\/General\/match2.htm<\/a>). This activity challenges your ability to recognize organic figures that might be the same. Write something here certifying that you completed this learning activity.<\/li>\r\n<\/ol>","rendered":"
          \n
        1. Write the chemical formula, and Lewis structure for each of the following hydrocarbons:<\/li>\n<\/ol>\n

          (a) pentane<\/p>\n

          (b) 3-ethylhexane<\/p>\n

          (c) cis-4-hepten-1-ol<\/p>\n

          (d) 4-methyl-1-hexene<\/p>\n

          (e) 2-heptyne<\/p>\n

          (f) 3,4-dimethyl-1-octyne<\/p>\n

            \n
          1. Describe the difference between a saturated and unsaturated hydrocarbon. What would the hybridization be at the crucial carbons in each kind of molecule?<\/li>\n
          2. Write a condensed structural formula, such as CH3CH3, and describe the molecular geometry at each carbon atom.<\/li>\n<\/ol>\n

            (a) propene<\/p>\n

            (b) 1-butanol<\/p>\n

            (c) ethyl propyl ether<\/p>\n

            (d) cis-4-bromo-2-heptene<\/p>\n

            (e) 2,2,3-trimethylhexane<\/p>\n

            (f) formaldehyde<\/p>\n

              \n
            1. Write out the resonance structures for the acetate ion.<\/li>\n
            2. Complete the activity linked here<\/a> (https:\/\/www2.chemistry.msu.edu\/faculty\/reusch\/virttxtjml\/questions\/General\/match10.htm<\/a>) doing structure matching to formulas. Come back and type the letter answers in the order they appeared (Left to right).<\/li>\n
            3. Complete the activity linked here<\/a>. (https:\/\/www2.chemistry.msu.edu\/faculty\/reusch\/virttxtjml\/questions\/General\/match2.htm<\/a>). This activity challenges your ability to recognize organic figures that might be the same. Write something here certifying that you completed this learning activity.<\/li>\n<\/ol>\n","protected":false},"author":17533,"menu_order":8,"template":"","meta":{"_candela_citation":"[]","CANDELA_OUTCOMES_GUID":"","pb_show_title":"on","pb_short_title":"","pb_subtitle":"","pb_authors":[],"pb_section_license":""},"chapter-type":[],"contributor":[],"license":[],"class_list":["post-7894","chapter","type-chapter","status-publish","hentry"],"part":2958,"_links":{"self":[{"href":"https:\/\/courses.lumenlearning.com\/chemistryformajors\/wp-json\/pressbooks\/v2\/chapters\/7894","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/courses.lumenlearning.com\/chemistryformajors\/wp-json\/pressbooks\/v2\/chapters"}],"about":[{"href":"https:\/\/courses.lumenlearning.com\/chemistryformajors\/wp-json\/wp\/v2\/types\/chapter"}],"author":[{"embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/chemistryformajors\/wp-json\/wp\/v2\/users\/17533"}],"version-history":[{"count":1,"href":"https:\/\/courses.lumenlearning.com\/chemistryformajors\/wp-json\/pressbooks\/v2\/chapters\/7894\/revisions"}],"predecessor-version":[{"id":7895,"href":"https:\/\/courses.lumenlearning.com\/chemistryformajors\/wp-json\/pressbooks\/v2\/chapters\/7894\/revisions\/7895"}],"part":[{"href":"https:\/\/courses.lumenlearning.com\/chemistryformajors\/wp-json\/pressbooks\/v2\/parts\/2958"}],"metadata":[{"href":"https:\/\/courses.lumenlearning.com\/chemistryformajors\/wp-json\/pressbooks\/v2\/chapters\/7894\/metadata\/"}],"wp:attachment":[{"href":"https:\/\/courses.lumenlearning.com\/chemistryformajors\/wp-json\/wp\/v2\/media?parent=7894"}],"wp:term":[{"taxonomy":"chapter-type","embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/chemistryformajors\/wp-json\/pressbooks\/v2\/chapter-type?post=7894"},{"taxonomy":"contributor","embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/chemistryformajors\/wp-json\/wp\/v2\/contributor?post=7894"},{"taxonomy":"license","embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/chemistryformajors\/wp-json\/wp\/v2\/license?post=7894"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}